UnknownNot Applicable

Low Dose GnRHa Early Luteal Phase Down Regulation Versus GnRHa Ultra-short Protocol for Poor Ovarian Response

China200 participantsStarted 2016-12

Plain-language summary

The management of the poor responder patients is very difficult. Currently, there is no any standard treatment for poor responder patients. The study is designed to test a modified GnRHa protocol for poor ovarian response, low dose GnRHa early luteal phase down regulation, compare with GnRHa ultra-short protocol. This is a randomized controlled trial.

Who can participate

Age range35 Years – 45 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * At least two of the following three features must be present: i. Advanced maternal age (≥40 years) or any other risk factor for POR (poor ovarian response); ii. A previous POR (≤3 oocytes with a conventional stimulation protocol); iii. An abnormal ovarian reserve test (i.e. AFC \<7 follicles or AMH \<1.1 ng/ml). Exclusion Criteria: * Contraindications for IVF/ICSI * Contraindications for pregnancy * Primary ovarian insufficiency * AFC \<3 * PGD/PGS

What they're measuring

live birth

Timeframe: 3 years

Trial details

NCT IDNCT02940535

SponsorNavy General Hospital, Beijing

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-12

Contact for this trial

Wei Shang, Dr

shang.wei@163.com

View on ClinicalTrials.gov More Subfertility, Female trials