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NCT03473613

Cabergoline Versus Calcium Infusion in Ovarian Hyperstimulation Syndrome Prevention

Completed Phase 3 Last updated 29 March 2018
What this trial tests

Phase 3 trial testing Oral Cabergoline in Ovarian Hyperstimulation in 230 participants. Completed in 15 April 2017.

Timeline
1 October 2014
Primary endpoint
15 April 2017
15 April 2017

Quick facts

Lead sponsorBenha University
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment230
Start date1 October 2014
Primary completion15 April 2017
Estimated completion15 April 2017
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Benha University

Who can join

Adults 18 to 45, female only, with Ovarian Hyperstimulation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Benha University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03473613.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing