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Resveratrol as a Preventive Treatment of OHSS

Resveratrol as a Preventive Treatment of Ovarian Hyperstimulation Syndrome

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03446625
Acronym
RES-OHSS
Enrollment
70
Registered
2018-02-27
Start date
2018-03-13
Completion date
2019-06-01
Last updated
2019-08-20

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

Conditions

Infertility

Keywords

resveratrol, OHSS, PCOS

Brief summary

Evaluation of resveratrol treatment oh ovarian hyperstimulation syndrome in egg donors

Detailed description

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

Interventions

DRUGResveratrol

Resveratrol treatment (2 g/day) will be administered for 9 days, starting from oocyte maturation day.

DRUGPlacebo

Placebo treatment (2 g/day) will be administered for 9 days, starting from oocyte maturation day.

Sponsors

IVI Madrid
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

* Number of follicles greater than 12 mm after ovarian stimulation * Number of retrieved oocytes greater than 21

Exclusion criteria

* \>35 years-old * PCOS * Endometriosis * Systemic pathology * Positive serologies for HBV, HBC and HIV * Abnormal karyotype

Design outcomes

Primary

MeasureTime frameDescription
Serum VEGF levels1 daySerum determination of VEGF levels

Secondary

MeasureTime frameDescription
Hemoconcentration1 dayVolume of red blood cells measured in percentage
Serum estradiol levels1 daySerum determination of estradiol levels asessed in picograms per mililiter
Ascitis1 dayVolume of liquid in Douglas pouch asessed in mililiters

Countries

Spain

Outcome results

None listed

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