Trials / Completed
CompletedNCT03473613
Cabergoline Versus Calcium Infusion in Ovarian Hyperstimulation Syndrome Prevention
Comparison of Cabergoline Versus Calcium Infusion in Ovarian Hyperstimulation Syndrome Prevention:Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 230 (actual)
- Sponsor
- Benha University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
Giving oral Cabergoline or calcium infusion in women at high risk for developing ovarian hyperstimulation syndrome in context of assisted reproductive technologies aiming in its prevention
Detailed description
Women undergoing in vitro fertilization or intracytoplasmic sperm injection whom were at high risk for developing ovarian hyperstimuation syndrome were received either oral Cabergoline.5mg tablets for 7days starting on ovum pick up day and continued for 7days or received 10ml of 10%calcium gluconate in 200ml normal saline on ovum pick up day and continued for 4days
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Oral Cabergoline | Giving oral Cabergoline tablet 0.5 milligram daily starting on ovum pick up day and continued for seven days |
| DRUG | Calcium Gluconate | Giving 10 ml of 10 % calcium gluconate on 200 ml normal saline solution o.9% intravenously over thirty minutes starting on ovum pick up day and continued for four days |
Timeline
- Start date
- 2014-10-01
- Primary completion
- 2017-04-15
- Completion
- 2017-04-15
- First posted
- 2018-03-22
- Last updated
- 2018-03-29
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT03473613. Inclusion in this directory is not an endorsement.