NCT Number: NCT02784457
Gonadotropin Releasing Hormone Antagonist in Treatment of Early-onset Severe Ovarian Hyperstimulation Syndrome
Efficacy of the use of GnRH antagonist in treatment of those who develop early-onset severe ovarian hyperstimulation syndrome and had cancelled embryo transfer
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Notify MeKey information
Conditions
Age range
20 year–42 year
Sex eligibility
Female
Study type
Interventional
Phase
Phase 2
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Women who develop early-onset severe ovarian hyperstimulation syndrome after controlled ovarian stimulation using long GnRH agonist protocol and hCG for triggering ovulation.
Exclusion criteria
- Women on short or antagonist protocols.
- Women who received GnRH agonist for triggering ovulation.
- Women who had embryo transfer.
Treatment and study plan
Primary outcomes
-
Number of women who needed culdocentesis or paracentesis of the ascitic fluid
Time frame: within 2 weeks of onset
Secondary outcomes
-
Number of women who needed hospitalization
Time frame: within 2 weeks of onset of symptoms
-
Time to regression of nausea/vomiting
Time frame: within 2 weeks of onset of symptoms
-
Time to regression of large ovarian size
Time frame: within 4 weeks of onset of symptoms
Sponsors and collaborators
Lead sponsor
Ain Shams University
Other
Registry information
Official study title
Gonadotropin Releasing Hormone Antagonist in Treatment of Early-onset Severe Ovarian Hyperstimulation Syndrome - a Randomized Controlled Trial
Important dates
- Study start
- 2014
- Primary completion
- 2015
- Study completion
- 2016
- First posted
- May 27, 2016
- Registry last updated
- May 27, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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