Clinical Trials Directory

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

TypeNameDescription
DRUGOral CabergolineGiving oral Cabergoline tablet 0.5 milligram daily starting on ovum pick up day and continued for seven days
DRUGCalcium GluconateGiving 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.