Prospective randomised study comparing luteal phase support in in-vitro fertilisation/intracytoplasmic sperm injection patients for three weeks versus seven weeks from day of positive pregnancy test

Completed

• Conditions: Infertility patients treated by IVF/ICSI; Pregnancy and Childbirth; Infertility

• Registration Number: ISRCTN88722916
• Lead Sponsor: The Egyptian IVF-ET Center (Egypt)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2007-01-25
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 400

Inclusion Criteria

1. Patients undergoing IVF/intra-cytoplasmic sperm injection (ICSI)
2. Aged less than 39 years
3. Having at least three high quality embryos

Exclusion Criteria

Intra-cytoplasmic sperm injection (ICSI) using surgically retrieved sperm.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Miscarriage rate in the first trimester

Secondary Outcome Measures

Name	Time	Method
1. Bleeding episodes in the first trimester<br>2. Adverse reactions to progesterone<br>