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The Novel Immunomodulatory and Anticoagulant Therapies for Recurrent Pregnancy Loss

The Novel Immunomodulatory and Anticoagulant Therapies for Recurrent Pregnancy Loss

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02990403
Enrollment
500
Registered
2016-12-13
Start date
2014-10-31
Completion date
2018-12-22
Last updated
2017-03-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent Pregnancy Loss

Brief summary

In this clinical cohort study, the investigators are going to observe the efficacy of anti-coagulation and immune therapy in the treatment of recurrent pregnancy loss with a prospective randomized controlled trial.

Interventions

DRUGAspirin
DRUGHeparin
DRUGPrednisone

Sponsors

Shanghai First Maternity and Infant Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

\- Woman who had 2 miscarriage before 12(th) week of gestation.The patient who is diagnosed as thrombophilia with recurrent pregnancy loss. Signed consent form.

Exclusion criteria

1. having experienced severe allergies, trauma history and/or operation history within 3 months. 2. with a history of mental illness and/or family history of mental illness limb disabled. 3. taking medicine within one month. 4. suffering major events or having mood swings. 5. having internal and surgical disease(after having variety of physical examination such as electrocardiogram/hepatic and renal function/blood routine and urine routine) 6. chromosome aberrations in anyone of the couple. 7. patients who have drugs contraindications

Design outcomes

Primary

MeasureTime frameDescription
live birththrough study completion, an average of 3 yearlive birth means success pregnancy(more than gestational age of 20 weeks)

Secondary

MeasureTime frame
D-dimerthrough study completion, an average of 3 year
Uterine artery blood flowthrough study completion, an average of 3 year
human chorionic gonadotropinthrough study completion, an average of 3 year

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026