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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
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03473613
Enrollment
230
Registered
2018-03-22
Start date
2014-10-01
Completion date
2017-04-15
Last updated
2018-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovarian Hyperstimulation

Keywords

Calcium infusion, Cabergoline

Brief 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

Interventions

Giving oral Cabergoline tablet 0.5 milligram daily starting on ovum pick up day and continued for seven days

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

Sponsors

Benha University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* women undergoing assisted reproductive technologies whom at high risk for developing ovarian hyperstimulation syndrome as with high basal antimullerian hormone ,excess antral follicular count ,high seum estradiol on day of humian choronic gonadotrophin

Exclusion criteria

women with other endocrinopathy as congenital adrenal hyperplasia , hyperprolactinemia,diabetes \-

Design outcomes

Primary

MeasureTime frameDescription
Occurrence of ovarian hyperstimuation syndrome20 days from ovum pick up dayClinical condition occurred in context of assisted reproductive technologies in which there serous sacs fluid accumulation and hemoconcentration

Secondary

MeasureTime frameDescription
Types of ovarian hyperstimuation syndrome and severity20 days from ovum pick up dayClinical severity either mild ,moderate or severe and its type either early or late onst
Chemical pregnancy14 day from embryos transfer dayPositive human chorionic Gonadotropin in blood
Clinical pregnancy5 week from embryos transfer dayIntrauterine gestational sac

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026