Peking University Insititute of Hematology, Peking University People's Hospital
Beijing, Beijing Municipality, 100010, China
Location status: Recruiting
NCT Number: NCT06577909
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.
Interested in participating?
Request Info18 year–50 year
Female
Interventional
Phase 2
Beijing, Beijing Municipality, 100010, China
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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 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
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
Time frame: 4 weeks
Platelet count ≥100×10^9/L measured on 2 occasions at least 7 days apart and the absence of bleeding
Time frame: 1 week
Platelet count ≥30×10^9/L and at least doubling baseline at 1 week
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
Time frame: 4 weeks
The day achieving OR
Time frame: 1 year
The time from achievement of CR or R to time of relapse
Time frame: At delivery
Platelet counts at delivery
Time frame: up to 42 days per newborn
Platelet counts of d1, 3, and 7 of newborns, extended to d42 if thrombocytopenia occurs
Time frame: 2 years
up to 2 years per subject
Interested in participating?
Request InfoPeking University People's Hospital
Other
Prednisone Plus IVIg Compared With Prednisone for Immune Thrombocytopenia During Pregnancy
Acronym: IVIg
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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