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Completed

NCT Number: NCT02633878

Chinese Herbal Medicine (New "Shoutai Wan") and/or Oral Progesterone Intervention Trial for Threatened Miscarriage

Threatened miscarriage is manifested by vaginal bleeding, with or without abdominal pain, while the cervix is closed and the fetus is viable and inside the uterine cavity. Threatened miscarriage is a common complication of pregnancy occurring in 20% of all clinically recognized pregnancies and about half of these will eventually result in pregnancy loss. The goal of this two by two factorial, placebo controlled randomized trial is to determine that two oral medications and their combination, will mostly likely result in live birth in women with threatened miscarriage. We will evaluate the efficacy and safety of Chinese herbal medicine (New "Shoutai Wan", NSTW) and/or oral micronized progesterone (OP) for treating threatened miscarriage in this trial. Our primary outcome of this trial is live birth. We hypothesize that: 1. treatment with NSTW plus OP or OP placebo is more likely to result in live birth than NSTW placebo plus OP or placebo; 2. treatment with OP plus NSTW or NSTW placebo is more likely to result in live birth than OP placebo plus NSTW or NSTW placebo; 3. treatment with combination of NSTW and OP is more likely to result in live birth than combination of NSTW placebo and OP placebo.

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Key information

Age range

20 year–37 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, Anhui, China

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About this study

The causes of spontaneous miscarriage are diverse and comprise chromosomal, genetic, anatomical, immunological, hormonal, infectious and psychological factors, the other factors contribute to an increased risk include advancing paternal and maternal age and mothers with systemic diseases, such as diabetes or thyroid dysfunction. The incidence is difficult to determine precisely because it occurs very early during a pregnancy and almost 30% of early pregnancy may go unrecognized; the pathogenesis of pregnancy loss in this condition is still remains obscure. Compared with healthy women, the women with threatened miscarriage were found not only to have increased rate of antepartum haemorrhage, prelabour rupture of the membranes, preterm delivery, and intrauterine growth restriction, but also suffer from significant psychological impairment including considerable anxiety and stress, depression, sleep disturbances, anger, and marital disturbances.

To date, therapies have limited effectiveness in treating threatened miscarriage and are empirical. Bed rest does not prevent pregnancy loss. Acetaminophen may have some effects on relieving pain only. The most commonly used prescription medication was human chorionic gonadotropin (hCG), maintaining the luteotrophic effects to support continued secretion of estrogen and progesterone, but it's beneficial effects still cannot be verified. Progesterone is another most commonly used standard medication, maintaining the endometrial proliferation and preventing poor decidualization. A number of recent studies in women with threatened miscarriage shown a reduction in pregnancy loss with progesterone treatment. But progestogens are a group of hormones, including both the natural female sex hormone progesterone and the synthetic forms. Micronized progesterone is a kind of progesterone; it is structurally and pharmacologically very similar to natural progesterone and has good oral bioavailability. It is especially suitable for women with threatened miscarriage as it does not have androgenic or oestrogenic effects on the foetus. A recent review of maternal use of micronized progesterone during pregnancy also found no evidence for an increased risk of congenital malformations. However it may only be suitable to treat women with threatened miscarriage who have low progesterone levels due to corpus luteum deficiency at the first trimester of pregnancy. There is no evidence to show the beneficial effects of progesterone to treat threatened miscarriage due to others factors. At the same time, progesterone treatment is also expensive. New or adjuvant treatments that are suitable, readily accessible, affordable, and safe are needed to treat women with threatened miscarriage.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age of women between 20-37 years.
  • Pregnant. The fetus is viable inside the uterine cavity during early pregnancy (5-10 week gestations) by ultrasound and/or serum hCG changes.
  • Bleeding symptoms: vaginal bleeding with or without abdominal pain, while the cervix is closed in during speculum examination.

Exclusion criteria

  • Multiple pregnancies (more than one gestational sac or fetal pole in ultrasonography).
  • Ectopic pregnancy. We will define an ectopic pregnancy as any suspected adnexal mass or large amounts of free fluid in the pelvis without an accompanying intrauterine pregnancy.
  • Pregnancies of Unknown Location (PUL). This will include pregnancies with an hCG level >2500mIU/mL without visualization of an intrauterine or extrauterine (i.e. ectopic) pregnancies.
  • Non-viable pregnancy. We will define a non-viable pregnancy as: (1) an intrauterine pregnancy with a fetal pole without visualized fetal heart motion (>49 days); (2) a gestational sac>20 mm in any diameter without a yolk sac; (3) absence of a normal gestational sac at 5 weeks of pregnancy, absence of a yolk sac at 5.5-6 weeks of pregnancy, or absence of cardiac activity at 7 weeks of pregnancy by ultrasound; (4) falling serum hCG values on serial visits or between baseline and randomization visit, or serial serum hCG levels which show a plateau (2-day increase ≤ 10%).
  • Intrauterine abnormalities or submucosal fibroids distorting uterine cavity (as assessed by ultrasound).
  • Bleeding attributed to a vulvar, vaginal, or cervical source unrelated to the pregnancy.
  • For this threatened miscarriage, use of the same or similar Chinese medicine and/or progesterone more than one week.
  • History of a congenital or acquired bleeding diathesis, i.e. Hemophilia, Von Willebrands's Disease, use of anti-coagulants, etc.
  • Presence of contributing major medical disorders (regardless of severity). These include poorly controlled diabetes, uncontrolled hypertension, systemic lupus erythematosus (SLE), untreated or active cancer (any cancer in remission or non-melanoma skin cancer is not included in the exclusion criteria), liver disease, renal disease, rheumatoid arthritis, cardiac disease, pulmonary disease other than mild asthma, neurologic disease requiring medical treatment, uncontrolled hypothyroidism, uncontrolled seizure disorder. Untreated vitamin B12 deficiency, severe anemia (hct < 30%), hemophilia, gout, nasal polyps.
  • Known current or recent alcohol abuse or illicit drug use.
  • Known abnormal parental karyotype.
  • Unwilling to give informed consent.

Treatment and study plan

Chinese Herbal Medicine (New "Shoutai Wan") plus Oral Progesterone

Drug

Chinese Herbal Medicine (New "Shoutai Wan", one pack twice daily) + Oral Progesterone (100 mg thrice daily)

Chinese Herbal Medicine (New "Shoutai Wan") plus Oral Progesterone Placebo

Drug

Chinese Herbal Medicine (New "Shoutai Wan", one pack twice daily) + Oral Progesterone Placebo (100 mg thrice daily)

Chinese Herbal Medicine Placebo (New "Shoutai Wan" placebo) plus Oral Progesterone

Drug

Chinese Herbal Medicine Placebo (New "Shoutai Wan" placebo, one pack twice daily) + Oral Progesterone (100 mg thrice daily)

Chinese Herbal Medicine Placebo (New "Shoutai Wan" placebo) plus Oral Progesterone Placebo

Drug

Chinese Herbal Medicine Placebo (New "Shoutai Wan" placebo, one pack twice daily) + Oral Progesterone Placebo (100 mg thrice daily)

Primary outcomes

  1. Live birth

    Time frame: At or beyond 20 completed weeks' gestation

    Rate of live birth at or beyond 20 completed weeks' gestation

Secondary outcomes

  1. Pregnancy outcome: Ongoing pregnancy

    Time frame: Beyond 12 weeks' gestation

    Rate of ongoing pregnancy (beyond 12 weeks' gestation)

  2. Pregnancy outcome: Miscarriage during the first trimester

    Time frame: During the first trimester (at or before 12 weeks' gestation)

    Rate of miscarriage during the first trimester (at or before 12 weeks' gestation)

  3. Pregnancy outcome: Miscarriage during second and third trimesters

    Time frame: During second and third trimesters (beyond 12 weeks' gestation until 20 weeks)

    Rate of miscarriage during second and third trimesters (beyond 12 weeks' gestation until 20 weeks)

  4. Pregnancy outcome: Termination

    Time frame: At any time during treatment (up to 2 months) and follow-up period (up to 1 year)

    Rate of termination at any time during treatment and follow-up period

  5. Pregnancy outcome: Stillbirth

    Time frame: At or beyond 20 weeks' gestation

    Rate of stillbirth (at or beyond 20 weeks' gestation)

  6. Pregnancy outcome: Induced abortion

    Time frame: At any time during treatment (up to 2 months) and follow-up period (up to 1 year)

    Rate of induced abortion at any time during treatment and follow-up for any reasons

  7. Pregnancy outcome: Gestational age at delivery

    Time frame: Up to 1 day after delivery

    Gestational age at delivery (weeks and days)

  8. Pregnancy outcome: Preterm birth

    Time frame: Birth before 37 completed weeks' gestation (up to and including 36 weeks and 6 days of gestation)

    Rate of preterm birth (birth beyond 28 week and before 37 completed weeks' gestation (up to and including 36 weeks and 6 days of gestation))

  9. Pregnancy outcome: Extreme preterm birth

    Time frame: Birth beyond 20 weeks and before 28 completed weeks' gestation (up to and including 27 weeks and 6 days of gestation)

    Rate of extreme preterm birth (birth beyond 20 weeks and before 28 completed weeks' gestation (up to and including 27 weeks and 6 days of gestation))

  10. Pregnancy outcome: Full-term birth

    Time frame: At or beyond 37 weeks' gestation, and before 42 weeks' gestation

    Rate of full-term birth (at or beyond 37 weeks' gestation, and before 42 weeks' gestation)

  11. Pregnancy outcome: Post-term birth

    Time frame: At or beyond 42 weeks' gestation

    Rate of post-term birth (at or beyond 42 weeks' gestation)

  12. Neonatal outcome: Birth weight

    Time frame: When neonatal is born

    Birth weight of neonatal (adjusted for gestational age and sex by Chinese standards)

  13. Neonatal outcome: Small for gestational age

    Time frame: When neonatal is born

    Rate of small for gestational age when neonatal is born

  14. Neonatal outcome: Large for gestational age

    Time frame: When neonatal is born

    Rate of large for gestational age when neonatal is born

  15. Neonatal outcome: Congenital malformation

    Time frame: At any time during treatment (up to 2 months) and follow-up period (up to 1 year)

    Rate of congenital malformation

  16. Other outcome: Mean score change in TCM Symptom Questionnaire

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months

    Mean score change in TCM Symptom Questionnaire from baseline to the end of intervention. The questionnaire covers many dimensions including symptoms (amount of vaginal bleeding, severity of abdominal pain and other general symptoms), emotional factors and so on. The minimum and maximum value are depend on the symptoms of the patient respectively.

  17. Other outcome: Mean score change in 12-Item Short-Form Health Survey

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months

    Mean score change in 12-Item Short-Form Health Survey from baseline to the end of intervention. The minimum value is 0 and the maximum value is 100, and higher scores mean a better outcome.

  18. Other outcome: Mean score change in Self-Rating Anxiety Scale

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months

    Mean score change in Self-Rating Anxiety Scale from baseline to the end of intervention. The minimum value is 20 and the maximum value is 80, and lower scores mean a better outcome.

Other outcomes

  1. Safety outcomes: Serious adverse events - Acute kidney injury (AKI)

    Time frame: At any time during treatment (up to 2 months) and follow-up period (up to 1 year)

    Rate of acute kidney injury (AKI)

  2. Safety outcomes: Serious adverse events - Drug induced liver injury (DILI)

    Time frame: At any time during treatment (up to 2 months) and follow-up period (up to 1 year)

    Rate of drug induced liver injury (DILI)

  3. Safety outcomes: Serious adverse events - Hospitalization

    Time frame: At any time during treatment (up to 2 months) and follow-up period (up to 1 year)

    Rate of hospitalization (for threatened abortion in second and third trimester of pregnancy, hyperemesis gravidarum, aggravation-vaginal bleeding, cervical polypectomy, fall injuries and other reasons)

  4. Safety outcomes: Adverse events - Nausea and vomiting

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of nausea and vomiting.

  5. Safety outcomes: Adverse events - Dizziness

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Dizziness.

  6. Safety outcomes: Aadverse events - Fetal and neonatal complications

    Time frame: From date of randomization until the date of end of pregnancy

    Rate of fetal and neonatal complications. Fetal complications including distress, and neonatal complications including early infection, NICU admission, pneumonia, hyperbilirubinemia.

  7. Safety outcomes: Adverse events - Fatigue

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Fatigue.

  8. Safety outcomes: Adverse events - Anorexia

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Anorexia.

  9. Safety outcomes: Adverse events - Constipation

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Constipation.

  10. Safety outcomes: Adverse events - Breast distention and pain

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Breast distention and pain

  11. Safety outcomes: Adverse events - Upper respiratory tract infection

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Upper respiratory tract infection.

  12. Safety outcomes: Adverse events - Abdominal pain

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Abdominal pain

  13. Safety outcomes: Adverse events - Somnolence

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Somnolence

  14. Safety outcomes: Adverse events - Insomnia

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Insomnia

  15. Safety outcomes: Adverse events - Anemia

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Anemia

  16. Safety outcomes: Adverse events - Diarrhea

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Diarrhea

  17. Safety outcomes: Adverse events - Suspected acute kidney injury (AKI)

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Suspected acute kidney injury (AKI)

  18. Safety outcomes: Adverse events - Suspected drug-induced liver injury (DILI).

    Time frame: From date of randomization until the date of end of treatment, assessed up to 2 months.

    Rate of Suspected drug-induced liver injury (DILI).

  19. Safety outcomes: Maternal complications - Pregnancy induced hypertension

    Time frame: From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks.

    Rate of Pregnancy induced hypertension

  20. Safety outcomes: Maternal complications - Pre-eclampsia

    Time frame: From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks.

    Rate of Pre-eclampsia

  21. Safety outcomes: Maternal complications - Gestational diabetes mellitus

    Time frame: From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks.

    Rate of Gestational diabetes mellitus

  22. Safety outcomes: Maternal complications - Placenta previa

    Time frame: From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks.

    Rate of Placenta previa

  23. Safety outcomes: Maternal complications - Pre-labour rupture of membranes

    Time frame: From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks.

    Rate of Pre-labour rupture of membranes

  24. Safety outcomes: Maternal complications - Postpartum haemorrhage

    Time frame: From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks.

    Rate of Postpartum haemorrhage

  25. Safety outcomes: Fetal complications - Fatal distress

    Time frame: From the date of end of treatment until the date of end of pregnancy, assessed up to 34 weeks.

    Rate of Fatal distress

  26. Safety outcomes: Neonatal complications - Neonatal Early infection

    Time frame: From the date of delivery, assessed up to 6 weeks

    Rate of Neonatal Early infection

  27. Safety outcomes: Neonatal complications - Neonatal NICU admission

    Time frame: From the date of delivery, assessed up to 6 weeks

    Rate of Neonatal NICU admission

  28. Safety outcomes: Neonatal complications - Neonatal pneumonia

    Time frame: From the date of delivery, assessed up to 6 weeks

    Rate of Neonatal pneumonia

  29. Safety outcomes: Neonatal complications - Neonatal hyperbilirubinemia

    Time frame: From the date of delivery, assessed up to 6 weeks

    Rate of Neonatal hyperbilirubinemia

Sponsors and collaborators

Lead sponsor

Heilongjiang University of Chinese Medicine

Other

Registry information

Official study title

Chinese Herbal Medicine (New "Shoutai Wan") and/or Oral Progesterone Intervention Trial for Threatened Miscarriage (CHOP-IT): An International Cooperative Multicenter Randomized Controlled Trial

Important dates

Study start
2017
Primary completion
2025
Study completion
2025
First posted
Dec 17, 2015
Registry last updated
Jan 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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