Clinical Trials Directory

Trials / Completed

CompletedNCT02875587

Cabergoline Versus Calcium Gluconate Infusion in the Prevention of Ovarian Hyperstimulation Syndrome

Cabergoline Versus Calcium Gluconate Infusion in the Prevention of Ovarian Hyperstimulation Syndrome. A Randomized Controlled Trial

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
170 (actual)
Sponsor
Aljazeera Hospital · Academic / Other
Sex
Female
Age
18 Years – 37 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to compare the efficacy of calcium gluconate infusion versus cabergoline in the prevention of ovarian hyperstimulation syndrome (OHSS) in patients pretreated with GnRH agonist long protocol who are at high risk for OHSS.

Detailed description

Ovarian hyperstimulation syndrome (OHSS) is a serious complication of assisted reproduction. Previous studies revealed that calcium gluconate infusion reduced the risk of OHSS. Other studies revealed that cabergoline (potent dopamine receptor agonist on D2 receptors)was effective in preventing OHSS. The aim of this study is to compare the efficacy of calcium gluconate infusion versus cabergoline in the prevention of ovarian hyperstimulation syndrome (OHSS) in patients pretreated with GnRH agonist long protocol who are at high risk for OHSS.

Conditions

Interventions

TypeNameDescription
DRUGCabergolineCabergoline (Dostinex; Pfizer, Italy) at a daily dose of 0.5 mg is administered orally at bed time for 8 days starting on the day of HCG administration
DRUGCalcium gluconateIntravenous 10% calcium gluconate, 10 mL in 200 mL of physiologic saline on the day of ovum pickup, day 1, day 2, and day 3 after ovum pickup. Intravenous infusion will be performed within 30 minutes.

Timeline

Start date
2016-10-01
Primary completion
2018-08-01
Completion
2018-12-01
First posted
2016-08-23
Last updated
2018-12-27

Locations

2 sites across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02875587. Inclusion in this directory is not an endorsement.