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RecruitingNCT06739759

Ovarian Hyperstimulation Syndrome Prevention

Prophylaxis Against Ovarian Hyperstimulation Syndrome in PCOS Women

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Aljazeera Hospital · Academic / Other
Sex
Female
Age
19 Years – 42 Years
Healthy volunteers
Not accepted

Summary

Ovarian hyperstimulation is a very hazardous complication of ICSI

Detailed description

Ovarian hyperstimulation could be mild , moderate , severe or marked

Conditions

Interventions

TypeNameDescription
DRUGAntagonist protocol for IVFantagonist protocol with triggering by Decapeptyl
DRUGModified Agonist protocol for IVF with additive treatments as HCQgiving additive drugs to agonist protocolas HCQ

Timeline

Start date
2024-11-17
Primary completion
2025-06-30
Completion
2025-07-30
First posted
2024-12-18
Last updated
2024-12-18

Locations

2 sites across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06739759. Inclusion in this directory is not an endorsement.

Ovarian Hyperstimulation Syndrome Prevention (NCT06739759) · Clinical Trials Directory