Ivi Madrid
Madrid, 28023, Spain
NCT Number: NCT03446625
Evaluation of resveratrol treatment oh ovarian hyperstimulation syndrome in egg donors
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Notify Me18 year–35 year
Female
Interventional
Phase 3
Madrid, 28023, Spain
Randomized clinical trial to evaluate the role of resveratrol in preventing ovarian hyperstimulation syndrome by reducing VGEF expression and estradiol production, imporving hemoconcentration and symptomathology of this condition
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Resveratrol treatment (2 g/day) will be administered for 9 days, starting from oocyte maturation day.
Other names: Resverasor Plus
Placebo treatment (2 g/day) will be administered for 9 days, starting from oocyte maturation day.
Time frame: 1 day
Serum determination of VEGF levels
Time frame: 1 day
Volume of red blood cells measured in percentage
Time frame: 1 day
Serum determination of estradiol levels asessed in picograms per mililiter
Time frame: 1 day
Volume of liquid in Douglas pouch asessed in mililiters
IVI Madrid
Other
Resveratrol as a Preventive Treatment of Ovarian Hyperstimulation Syndrome
Acronym: RES-OHSS
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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