CompletedPhase 4

IVF/ICSI Protocols in Poor Responders With Growth Hormone

Egypt287 participantsStarted 2013-07

Plain-language summary

in this study, we are trying to monitor the effect of the addition of growth hormone on the different down regulation protocols ( long, short, antagonist and microflare). The outcome will be primarily assessed by the clinical pregnancy rates.

Who can participate

Age range20 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: ESHRE consensus 2011,At least two of the following three features must be present: * Advanced maternal age (≥40 years) or any other risk factor for POR; * A previous POR (≤3 oocytes with a conventional stimulation protocol); * An abnormal ovarian reserve test (i.e. AFC \< 5-7 follicles or AMH \< 0.5 -1.1 ng/ml). Exclusion Criteria: * female patients with causes of infertility other than poor ovarian reserve * females suffering from congenital or acquired uterine anomalies * females with focal uterine lesions * females who had previous ovarian surgeries * females with history of previous exposure to radiotherapy , or chemotherapy * females refusing to get enrolled in the study

What they're measuring

Numbers of oocytes retrieved and number of fertilized oocytes

Timeframe: 2 years

Trial details

NCT IDNCT01897324

SponsorWoman's Health University Hospital, Egypt

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-01

View on ClinicalTrials.gov More Female Infertility Due to Diminished Ovarian Reserve trials