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NCT Number: NCT05290558

The Therapeutic Effects of Bu Shen Yi Jing Pill on Semen Quality in Sub Fertile Males: a Randomized Controlled Trial

This study aims to evaluate the safety and efficacy of Bu Shen Yi Jing (BSYJ) Pill , a type of traditional Chinese medicine, in improving male subfertility and semen parameters.

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Key information

Age range

21 year–49 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

KK Women's and Children's Hospital

Singapore, 229899

About this study

Subfertility is defined as a failure to conceive after 1 year of regular unprotected intercourse. Impaired fertility affects 10 to 15% of couples and male factor is the cause of subfertility in 25 to 40% of couples. With increasing paternal age, semen volume, sperm motility and the percentage of sperm with normal morphology decreases. The majority of men who present with subfertility have either abnormal sperm density, motility or morphology, or a combination of the above, and treatment for this condition is varied and empirical.

There is a paucity of studies and randomized controlled trials to guide treatment of male factor subfertility. Various antioxidant formulations and multivitamins have been used empirically but have not been shown consistently to improve sperm counts and viability. When treatment fails, assisted reproduction will be the last resort. All assisted reproduction treatments are associated with medical, financial and emotional burden. Given the lack of proven treatment options in Western Medicine, Traditional Chinese Medicine (TCM) may provide a viable complementary treatment option. One such option is the Bu Shen Yi Jing (BSYJ) pill.

A clinical observational study conducted by the team in Singapore Thong Chai Medical on subfertile male patients with poor sperm quality and a body constitution of Kidney Deficiency showed that 2 courses of BSYJ pill over a 6 months' duration resulted in successful conception of 33% of azoospermic male patients (n = 60). In a subgroup of patients where serial sperm analysis was available (n=10), the percentage of sperm with grade A motility increased from a median of 22.6 ± 2.4% pre-treatment to 35.1 ± 3.2% post treatment (p < 0.05); and the hyaluronic binding assay improved from 33.2 ± 2.4% to 72 ± 4.6% (p < 0.05). This suggests that BSYJ pills possibly works on improving the motility of the sperms in patients having the Kidney deficiency body constitution.

As such, this study aims to validate these hypotheses and anecdotal evidence by conducting a safety and efficacy study of the BSYJ pill on a prospective cohort.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Duration of subfertility (both primary and secondary) ≥ 1 year;
  • Any or combination of the three abnormal semen parameters, defined according to the 2010 WHO criteria, including
  • Oligozoospermia, with sperm concentration less than 15 x 10^6,
  • Teratozoospermia, with normal sperm morphology less than 4%, and
  • Asthenozoospermia, with total sperm motility less than 40%, or progressive sperm motility less than 32%.
  • Diagnosed with TCM syndrome of Kidney Deficiency Based on a prominent TCM diagnosis textbook known as TCM Diagnostics, the main symptoms patients need to fulfil for Kidney Deficiency are either nocturnal polyuria or lower back pain. In addition, patients need to fulfil any 1 of the secondary symptoms, including fatigue; dizziness; tinnitus or deafness; memory loss; excessive urination; low libido; wet dreams; premature ejaculation; presence of feverish palms and soles or night sweats; dry mouth or throat; cold intolerance or preference for warmth; poor sleep quality. Presence of both 1 main symptom and 1 secondary symptom allows for the diagnosis of the Kidney Deficiency syndrome.

Patients who meet all three criteria mentioned above will be included in the study.

Exclusion criteria

  • Azoospermia and severe oligoasthenoteratozoospermia;
  • Aspermia;
  • Varicocele;
  • Recent urogenital infections;
  • Y chromosome deletions;
  • Abnormal karyotypes
  • History of chemotherapy and / or radiotherapy;
  • Patients on fertility supplements or supplements marketed to improve fertility;
  • Patients with uncontrolled diabetes or/and hypertension; with uncontrolled chronic medical conditions
  • Patients currently already on BSYJ pills treatment

Treatment and study plan

Bu Shen Yi Jing Pill

Drug

Bu Shen Yi Jing Pill contained Radix Pseudostellaria, Fructus Lycii, Radix Et Rhizoma Salviae, Rhizoma Dioscorea, Semen Plantaginis, Semen Cuscuta, Patriniae Herba, Herba Epimedii, Radix Ophiopogonis, Fructus Rubi, Fructus Corni, Bupleurum roots, Fructus Schisandrae Chinensis, Radix Et Rhizoma Glycyrrhizae.

Dosage of the study drug is as follows: 3 pills each time, for 3 times a day, taken for 6 days every week for 1 year

Other names: BSYJ Pill

Placebo drug

Drug

Placebo contains the ingredients: grounded black rice and permitted colouring. The ingredients are encapsulated within a gelatine capsule.

Dosage of the study drug is as follows: 3 pills each time, for 3 times a day, taken for 6 days every week for 1 year

Other names: Control drug

Primary outcomes

  1. To determine the change in sperm volume from baseline after treatment with BSYJ pill

    Time frame: 1 year

    From sperm samples analyses

  2. To determine the change in sperm morphology from baseline after treatment with BSYJ pill

    Time frame: 1 year

    From sperm samples analyses

  3. To determine the change in sperm motility from the baseline after treatment with BSYJ pill

    Time frame: 1 year

    From sperm samples analyses

  4. To determine the change in sperm concentration from the baseline after treatment with BSYJ pill

    Time frame: 1 year

    From sperm samples analyses

Secondary outcomes

  1. To determine the clinical pregnancy rate and successful delivery rate after BSYJ pill

    Time frame: 2 year

    Defined by the number of pregnancies and subsequent actual births after commencement of BSYJ pill

  2. To study the safety and determine the changes in blood profile after treatment with BSYJ pill

    Time frame: 1 year

    Defined by changes in participant's full blood count, renal panel, liver function test and hormone profile.

Other outcomes

  1. To assess the common side effects of the BSYJ pill

    Time frame: 1 year

    Participant reported symptoms of excessive heat syndrome such as ulcers and mouth dryness.

  2. To assess the common gastrointestinal side effects of the BSYJ pill

    Time frame: 1 year

    Participant reported symptoms of gastrointestinal symptoms such as indigestion and appetite reduction.

  3. To evaluate safety profile of BSYJ pill

    Time frame: Up to 1 year after recruitment

    Participants will be assessed frequently to pick up any side effects noted after commencement of BSYJ pill

  4. Change from baseline severity based on TCM symptom scoring questionnaire

    Time frame: 1 year

    As BSYJ pills target the TCM syndrome of Kidney Qi deficiency, symptoms related to Kidney Qi deficiency syndrome, which includes frequent urination and back pain, fatigue and dizziness, may be improved through this research.

  5. Number of participants with improvement in TCM syndrome of Kidney Qi deficiency from baseline according to the TCM symptom scoring questionnaire Stagnation

    Time frame: 1 year

    As BSYJ pills target the TCM syndrome of Kidney Qi deficiency, symptoms related to Kidney Qi deficiency syndrome, which includes frequent urination and back pain, fatigue and dizziness, may be improved through this research.

  6. Patient's basic demographics

    Time frame: 1 year

    Defined by age, ethnicity, marital status

  7. Patient's partner's basic demographics

    Time frame: 1 year

    Defined by age, ethnicity, marital status

  8. Patients's anthropometry

    Time frame: 1 year

    Defined by height, weight and body mass index based on weight (kg) /height (m)2

  9. Number of participants who smoke

    Time frame: 1 year

    Self-reported

  10. Number of participants who take alcohol regularly

    Time frame: 1 year

    Self-reported based on the amount and frequency of alcohol intake

  11. Number of participants who have dietary restrictions

    Time frame: 1 year

    Self-reported

  12. Number of participants with occupational exposures to chemicals

    Time frame: 1 year

    Self-reported

  13. Number of participants with exposure to hot baths or jacuzzi

    Time frame: 1 year

    Self-reported

  14. Number of participants who uses recreational drugs

    Time frame: 1 year

    Self-reported

  15. Number of participants who exercise regularly

    Time frame: 1 year

    Self-reported

  16. Number of patients with significant medical history

    Time frame: 1 year

    Self-reported details of medical history

  17. Number of patients with significant surgical history

    Time frame: 1 year

    Self-reported details of surgical history

  18. Number of patients on regular medications

    Time frame: 1 year

    Self-reported details of types of regular medications

  19. Number of patients with drug allergies

    Time frame: 1 year

    Self-reported details of drug allergies

  20. Number of patients who take supplements

    Time frame: 1 year

    Self-reported details of the type of supplements taken

  21. Number of patients who take steroids

    Time frame: 1 year

    Self-reported

  22. Number of patients with previous history of sexually transmitted disease

    Time frame: 1 year

    Self-reported details of sexually transmitted disease

  23. Number of patients with previous history of genital trauma

    Time frame: Since birth

    Self-reported details of genital trauma

  24. Patient's fertility history

    Time frame: 1 year

    Determined by the number of years of attempts at conception, sexual intercourse frequency, number of paternity (including current and/or previous partners), previous fertility treatments and medications

  25. Patient's partner's fertility history

    Time frame: 1 year

    Determined by the number of years of attempts at conception, sexual intercourse frequency, number of maternity (including current and/or previous partners), previous fertility treatments and medications, and menstrual history

Sponsors and collaborators

Lead sponsor

KK Women's and Children's Hospital

Other Gov

Registry information

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Mar 22, 2022
Registry last updated
Oct 10, 2024

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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