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NCT Number: NCT06577909

Prednisone Plus IVIg vs. Prednisone for ITP During Pregnancy

This is a prospective, randomized, open-label, multicenter clinical trial study to compare the efficacy and safety of prednisone plus IVIg to prednisone monotherapy in the treatment of immune thrombocytopenia (ITP) in pregnancy.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Peking University Insititute of Hematology, Peking University People's Hospital

Beijing, Beijing Municipality, 100010, China

Location status: Recruiting

Location contact

Haixia Fu, MD

CONTACT

[email protected]

13581830157

Xiaohui Zhang, MD

CONTACT

[email protected]

+8613522338836

Xiaohui Zhang, MD

PRINCIPAL_INVESTIGATOR

About this study

The investigators are undertaking a prospective, parallel group, multicenter, randomized controlled trial in pregnant patients with treat-naive ITP. A total of 100 participants are randomized to two groups with the 1:1 ratio: prednisone plus IVIg group versus prednisone monotherapy group. Participants will receive prednisone 20mg per day for 4 weeks plus IVIg 400mg/Kg (total dose ≤20g per day) for 5 days or prednisone 20mg monotherapy per day for 4 weeks. Platelet count, bleeding and other symptoms were evaluated before and after treatment. Time to response and platelet counts of newborns are investigated. Adverse events including participants and their newborns are also recorded throughout and after the study.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18-50 years old;
  • Meet the diagnostic criteria for immune thrombocytopenia;
  • Pregnant women with ITP without ITP-specific treatments during pregnancy;
  • Gestational weeks ≥12 weeks;
  • Platelet count <30×10^9/L, accompanied with or without bleeding symptoms.
  • Willing and able to sign written informed consent.

Exclusion criteria

  • Have a known diagnosis of other autoimmune diseases, confirmed medical history or laboratory findings within positive anti-nuclear antibodies (>1:80), anti-cardiolipin antibodies, lupus anticoagulant factors or direct Coombs' test.
  • Thrombocytopenia caused by pregnancy-specific conditions, such as gestational thrombocytopenia, preeclampsia, the HELLP syndrome and acute fatty liver of pregnancy.
  • Secondary thrombocytopenia such as drug-related thrombocytopenia, vaccine-related thrombocytopenia, lymphoproliferative disorders, severe infection, hepatic cirrhosis and so on.
  • With other underlying diseases that may cause thrombocytopenia, such as: malignant disease, megaloblastic anemia, aplastic anemia, myelodysplasia syndrome, myeloid fibrosis, disseminated intravascular coagulation, thrombotic thrombocytopenic purpura, Hemolytic uremic syndrome, disseminated intravascular coagulation and so on;
  • Current HIV infection or hepatitis B virus or hepatitis C virus infections;
  • With severe heart, kidney, liver or respiratory dysfunction;
  • With the medical history of mental illness;
  • Have allergic reaction to prednisone or IVIg;

Treatment and study plan

Prednisone

Drug

Prednisone po, 20mg per day for 4 weeks, if response (Plt 30-100×100^g/L), gradually taper to the maintenance dose of 5-10mg per day until 6 weeks after delivery; if not response, gradually taper to withdrawal.

Other names: Pre

IVIG

Drug

IVIg 400mg/kg (≤20g for the total dose) per day for 5 days, and repeated in the case of lack of response by day 14

Other names: intravenous immunoglobulin

Primary outcomes

  1. Overall Response

    Time frame: 4 weeks

    Achieving a platelet count of≥30×10^9/L and at least a doubling of the baseline platelet count without administration of any other ITP-specific treatment, and the absence of bleeding

Secondary outcomes

  1. Complete Response

    Time frame: 4 weeks

    Platelet count ≥100×10^9/L measured on 2 occasions at least 7 days apart and the absence of bleeding

  2. Early response

    Time frame: 1 week

    Platelet count ≥30×10^9/L and at least doubling baseline at 1 week

  3. relapse

    Time frame: 1 year

    After the treatment is effective, the platelet count drops below 30×10^9/L or drops to less than 2 times the basal value, or bleeding symptoms occur

  4. Time to Response

    Time frame: 4 weeks

    The day achieving OR

  5. Time to relapse (duration of efficacy)

    Time frame: 1 year

    The time from achievement of CR or R to time of relapse

  6. Platelet counts at delivery

    Time frame: At delivery

    Platelet counts at delivery

  7. Platelet counts of newborns

    Time frame: up to 42 days per newborn

    Platelet counts of d1, 3, and 7 of newborns, extended to d42 if thrombocytopenia occurs

  8. Adverse events in parturients

    Time frame: 2 years

    up to 2 years per subject

Study contacts

Contact information is provided by the study sponsor or research team.

Haixia Fu, MD

CONTACT

[email protected]

13581830157

Xiaohui Zhang, Professor

CONTACT

[email protected]

+8613522338836

Sponsors and collaborators

Lead sponsor

Peking University People's Hospital

Other

Registry information

Official study title

Prednisone Plus IVIg Compared With Prednisone for Immune Thrombocytopenia During Pregnancy

Acronym: IVIg

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Aug 29, 2024
Registry last updated
Aug 29, 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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