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Ovarian Hyperstimulation Syndrome and Cabergoline

The Effect Of Cabergoline On Follicular Microenvironment Profile In Patients With High Risk Of Ohss

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01569256
Enrollment
40
Registered
2012-04-03
Start date
2008-03-31
Completion date
2009-03-31
Last updated
2012-04-04

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

Conditions

Ovarian Hyperstimulation Syndrome, Polycystic Ovarian Syndrome

Brief summary

Cabergoline prevents ovarian hyperstimulation syndrome in high risk patients by disrupting follicular fluid hormone microenvironmentally altering the follicular fluid levels of insulin like growth hormone -I (IGF-I), antimullerian hormone (AMH), inhibin B and hepatocyte growth factor (HGF) levels in women with PCOS and high risk of ovarian hyperstimulation syndrome (OHSS).

Detailed description

Dopamine agonists have been proposed as a prophylactic treatment for OHSS in women with high risk of OHSS, however the possible mechanism of action has not been clearly known. In experimental studies, inhibition of vascular endothelial growth factor based pathway was proposed as a possible action of mechanism of dopamine agonists. However the role hepatocyte growth factor (HGF), insulin like growth factor-I (IGF-I), inhibin B and antimullerian hormone (AMH) on cabergoline action in OHSS prevention has not been known.

Interventions

DRUGCabergoline

Cabergoline tablet, Pfizer, Istanbul, Turkey, started on day of HCG, 0.5 mg/day for 8 days

Sponsors

Etlik Zubeyde Hanim Womens' Health and Teaching Hospital
Lead SponsorUNKNOWN

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
23 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Development of more than 14 leading follicles larger than 10 mm and serum estradiol more than 3000 pg/ml at the end of ovulation induction with long luteal ovulation induction protocol. * Having the criteria of PCOS

Exclusion criteria

* Not having the inclusion criteria.

Design outcomes

Primary

MeasureTime frame
Concentrations of follicular fluid AMH1 year

Secondary

MeasureTime frame
Concentrations of follicular fluid inhibin B1 year
Concentrations of follicular fluid HGF1 year

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026