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Comparison of coasting with cabergoline administration for prevention of early severe Ovarian Hyper Stimulation Syndrome in Assisted Reproductive Technology cycles

Comparison of coasting with cabergoline administration for prevention of early severe Ovarian Hyper Stimulation Syndrome in Assisted Reproductive Technology cycles

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138706091132N1
Enrollment
60
Registered
2008-12-25
Start date
2006-07-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Ovarian Hyperstimulation Syndrome.

Interventions

Intervention 1: In coasting group, exogenous gonadotropins will be withheld to allow E2 to decrease while GnRH-a will be maintained. Then 10,000 Unit hCG will be administrated and oocyte retrieval wil
Prevention
In coasting group, exogenous gonadotropins will be withheld to allow E2 to decrease while GnRH-a will be maintained. Then 10,000 Unit hCG will be administrated and oocyte retrieval will be performed 3
In Cabergoline group, hCG will be administered and they receive 0.5 mg per day cabergoline orally from the day of hCG for 8 days. Luteal phase will be supported by administration of progesterone in oi

Sponsors

Research and Clinical Center for Infertility, Yazd Shahid Sadoughi University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 38 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with In Vitro Fertilization (IVF)/Intra Cytoplasmic Sperm Injection (ICSI) cycles who are at risk of developing OHSS. The definition of risk is: the presence of pre- ovulatory follicles = 20 in both ovaries.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Incidence of Severe OHSS. Timepoint: 2 weeks. Method of measurement: Clinical Management.

Secondary

MeasureTime frame
Implantation Rate. Timepoint: 2 weeks. Method of measurement: Number of gestational sacs per embryo transferred.;Clinical Pregnancy Rate. Timepoint: 2 weeks. Method of measurement: Embryonic cardiac activity observed by ultrasound.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactabbas aflatoonian

Research and Clinical Center for Infertility?Yazd Shahid Sadoughi University of Medical Sciences

abbas_aflatoonian@yahoo.com+98 35 1824 7085

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026