Cabergoline Versus Calcium Infusion in Ovarian Hyperstimulation Syndrome Prevention
Launched by BENHA UNIVERSITY · Mar 21, 2018
Trial Information
Current as of August 02, 2025
Completed
Keywords
ClinConnect Summary
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
Gender
FEMALE
Eligibility criteria
- 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
- • -
About Benha University
Benha University, a leading institution in Egypt, is dedicated to advancing medical research and innovation through rigorous clinical trials. With a strong emphasis on multidisciplinary collaboration, the university aims to enhance healthcare outcomes by exploring novel therapeutic approaches and interventions. Its state-of-the-art facilities and commitment to ethical research practices ensure that all trials are conducted with the highest standards of integrity and scientific rigor. Benha University actively contributes to the global medical community by fostering partnerships and disseminating findings that can improve patient care and inform public health policies.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Cairo, Elqalopia, Egypt
Patients applied
Trial Officials
Ashraf N Elmantwe, MD
Principal Investigator
Benha University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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