UnknownPhase 3NCT02620605

The Influence of Timing of Cabergoline Initiation on Prevention of OHSS

Studying Ovarian hyperstimulation syndrome

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Mona M Shaban
Principal Investigator
Mona M Shaban, MD
Intervention
Late Cabergoline 0.5mg(drug)
Enrollment
75 target
Eligibility
19-35 years · FEMALE
Timeline
20172019

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT02620605 on ClinicalTrials.gov

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