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NCT04026282: CLBR

To Investigate the Cumulative Live Birth Rates Using GnRH Antagonist or Agonist Protocol for COS in ART Treatment

Status unknown NA Last updated 8 November 2019
What this trial tests

NA trial testing GnRH-ant protocol in Sterility in 888 participants. Status unknown.

Timeline
27 December 2018
Primary endpoint
30 October 2021
31 July 2022

Quick facts

Lead sponsorPeking University Third Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment888
Start date27 December 2018
Primary completion30 October 2021
Estimated completion31 July 2022
Sites4 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking University Third Hospital

Who can join

Adults 18 to 38, female only, with Sterility. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a Phase IV, prospective, randomized controlled study to investigate the cumulative live birth rates (CLBRs) of gonadotrophin-releasing hormone (GnRH) antagonist protocol (GnRH-ant group) compared with the standard GnRH agonist long protocol (GnRH-a group) for controlled ovarian stimulation in supposed normal ovarian responders.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Peking University Third Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04026282.

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