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Clinical Trial Summary

A prospective study of the evaluation of the clinical IVF (in vitro fertilization) results after following Long Antagonist protocol for Controlled Ovarian Stimulation (COS) versus following Long Agonist protocol


Clinical Trial Description

A prospective study of the clinical results in women who followed the Long Antagonist protocol for Controlled Ovarian Stimulation (COS) versus women who followed Long Agonist protocol, in an In Vitro Fertilization (IVF) try. In particular, the Clinical Pregnancy Rates (CPR) and Live Birth Rates (LBR) were estimated for the two groups of patients. The number of the formed blastocysts was also measured in each group of patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03693534
Study type Observational
Source Assisting Nature
Contact Evaggelos Papanikolaou, MD,PhD
Phone 00302310424294
Email drvagpapanikolaou@yahoo.gr
Status Recruiting
Phase
Start date February 15, 2017
Completion date June 30, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT03463278 - The Number of Blastocysts Formed in the Outcome of Freeze All Strategy: COMFFETI Trial, Cumulative Delivery Rate
Completed NCT02442895 - Biomarkers of Ovarian Reserve and Correlation With IVF Treatments N/A
Completed NCT00773825 - Genomic Imprinting and Assisted Reproductive Technologies N/A
Recruiting NCT03240159 - Long Antagonist Protocol for IVF With Single Luteal Dose of Degarelix Phase 3
Recruiting NCT03684421 - Clinical and Live Birth Rates After Following Long Antagonist Protocol Versus Classical Antagonist Protocol