ACTRN12608000200381CompletedPhase 2
Effects of early luteal phase vaginal progesterone supplementation on the outcome of in-vitro fertilization and embryo transfer
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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