Clinical Trials Directory

Trials / Completed

CompletedNCT05281341

Effect of GH Administration in Poor Responders Undergoing Intracytoplasmic Sperm Injection (ICSI)

Effect of Growth Hormone Administration With Controlled Ovarian Stimulation in Expected Poor Responders POSEIDON Group 3 and 4 Undergoing ICSI Using Antagonist Protocol

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
160 (actual)
Sponsor
Alexandria University · Academic / Other
Sex
Female
Age
20 Years
Healthy volunteers
Not accepted

Summary

Despite the use of various treatment strategies, poor response to ovarian stimulation remains a major clinical challenge with lower chance to obtain sufficient number of oocytes and thus less likely to conceive with high risk of cycle cancellation. The aim of this study is to evaluate the effect of recombinant human GH administration to gonadotropins on clinical and laboratory ICSI outcomes in expected poor responders more and less than 35 years (Poseidon group 4 and 3 respectively).

Conditions

Interventions

TypeNameDescription
DRUGGrowth HormoneIn GH groups (Group 4A \& 3A), patients will receive additional treatment with GH (Somatropin, 4 IU/day, subcutaneous injection), daily beginning on the initial day of gonadotropin stimulation until triggering the oocyte maturation by hCG. Control groups (Group 4B \& 3B) will receive only standard COS without GH supplementation

Timeline

Start date
2020-01-13
Primary completion
2021-12-10
Completion
2022-02-13
First posted
2022-03-16
Last updated
2022-08-09

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05281341. Inclusion in this directory is not an endorsement.