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Clinical Trials/ACTRN12608000200381
ACTRN12608000200381CompletedPhase 2

Effects of early luteal phase vaginal progesterone supplementation on the outcome of in-vitro fertilization and embryo transfer

The Chinese University of Hong Kong0 sites196 target enrollmentStarted: April 14, 2008Last updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
196

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomised controlled trial
Primary Purpose
Treatment
Masking
Open (masking not used)

Eligibility Criteria

Ages
20 Years to 39 Years (—)
Sex
Female

Inclusion Criteria

  • women undergoing the treatment of in-vitro fertilization and embryo transfer, with HCG administration as the standard luteal phase support

Exclusion Criteria

  • age = 40 year-old
  • use of vaginal progesterone for luteal phase support because of risk of ovarian hyperstimulation syndrome
  • distorted uterine cavity, e.g. due to submucosal fibroids or uterine anomalies

Investigators

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