Clinical Trials Directory

Trials / Completed

CompletedNCT02271360

Calcium Dobesilate Versus Cabergoline for Prevention of Ovarian Hyperstimulation Syndrome

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
200 (actual)
Sponsor
Benha University · Academic / Other
Sex
Female
Age
22 Years – 44 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the effect of oral Calcium Dobesilate to oral Cabergoline in the prevention of ovarian hyperstimulation syndrome (OHSS) in high-risk women underwent intracytoplasmic sperm injection (ICSI).

Detailed description

Two hundred and twenty women at risk of ovarian hyperstimulation syndrome during ICSI cycles will be randomly scheduled into two equal groups. In group A, (Calcium Dobesilate group), 1 cap / 8 hs Doxium ( 500mg) will be given at day of HCG injection and for 21 days; while in group B (Cabergoline group), 1 tab/day Cabergoline( 0.5 mg) will be given at day of HCG injection and for 8 days.

Conditions

Interventions

TypeNameDescription
DRUGCalcium Dobesilate1 cap / 8 hs Calcium Dobesilate ( 500mg) will be given at day of HCG injection and for 21 days
DRUGCabergoline1 tab/day Cabergoline( 0.5 mg) will be given at day of HCG injection and for 8 days

Timeline

Start date
2014-04-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2014-10-22
Last updated
2017-02-16

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02271360. Inclusion in this directory is not an endorsement.