Overview

Habitual Abortion Study: Oral Dydrogesterone Treatment During Pregnancy in Women With Recurrent Miscarriage

Status:
Completed
Trial end date:
2009-07-01
Target enrollment:
0
Participant gender:
Female
Summary
The purpose of this clinical study is to demonstrate the shift from inflammatory cytokines to non-inflammatory cytokines in women suffering from habitual abortion treated with dydrogesterone (Duphaston).
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Abbott Products
Treatments:
Dydrogesterone
Criteria
Inclusion Criteria

- Women with a history of idiopathic recurrent miscarriage, based on a documented
history of at least three spontaneous consecutive miscarriages before 20 weeks
gestation with the same partner Exclusion Criteria

- Any verifiable cause of the recurrent miscarriages apart from luteal phase defect
(e.g. systemic lupus erythematosus [SLE], infections with chlamydia or mycoplasma)

- Any gynecological neoplasias or anatomical abnormalities that oppose pregnancy

- Concurrent infertility treatment/superovulation protocol