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
| Type | Name | Description |
|---|---|---|
| DRUG | Calcium Dobesilate | 1 cap / 8 hs Calcium Dobesilate ( 500mg) will be given at day of HCG injection and for 21 days |
| DRUG | Cabergoline | 1 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.