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Cabergoline and Hydroxyethyl Starch in Ovarian Hyperstimulation Syndrome Prevention

Prevention of Ovarian Hyperstimulation Syndrome in GnRH Agonist IVF Cycles: Randomized Study Comparing Hydroxyethyl Starch Versus Cabergoline and Hydroxyethyl Starch

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01530490
Enrollment
80
Registered
2012-02-10
Start date
2007-08-31
Completion date
2010-09-30
Last updated
2012-02-10

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

Conditions

Complications Associated With Artificial Fertilization, Disorder of Endocrine Ovary

Keywords

IVF, ovarian hyperstimulation syndrome, cabergoline, hydroxyethyl starch, prevention

Brief summary

The purpose of this study is to assess whether, in GnRH agonist in vitro fertilization (IVF) cycles, where there is a risk of ovarian hyperstimulation syndrome (OHSS), the addition of cabergoline to the hydroxyethyl starch infusion could decrease OHSS incidence and severity.

Detailed description

Women undergoing IVF cycles with GnRH agonist protocols, at risk of OHSS (more than 20 follicles observed larger than 12 mm in diameter and/or estradiol levels of 3000-5000 pg/mL). Slow infusion of 500 ml of 6% HES during follicular aspiration alone or combined with 0.5 mg cabergoline administration for 8 days, starting on the day of hCG administration.

Interventions

DRUGCabergoline and Hydroxyethyl Starch

0.5mg

0.5 mg cabergoline administration 8 days

Sponsors

Hospital de Cruces
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* to be at risk of OHSS were invited to participate in the study

Exclusion criteria

* age \> 40 years

Design outcomes

Primary

MeasureTime frame
risk of ovarian hyperstimulation syndrome12 days

Secondary

MeasureTime frame
pregnancy rate15 days

Outcome results

None listed

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