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Clinical Trial Summary

To compare the effect of Crinone 8% administered once daily versus other vaginal progesterone in terms of ongoing pregnancy rate 5 weeks after embryo transfer as well as patient convenience.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • IVF - Luteal Phase Support After Embryo Transfer

NCT number NCT00708539
Study type Interventional
Source Nordica Fertility Clinic
Contact Svend Lindenberg
Phone 004533257000
Email svend@lindenberg.dk
Status Recruiting
Phase Phase 4
Start date April 2006
Completion date December 2008