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Active Not Recruiting NCT03105518

Predictors of Postoperative Pain Following Oocyte Retrieval for Assisted Reproduction

Conditions: Oocyte Retrieval, Postoperative Pain

Sex: Female
Ages: 18 Years – 50 Years
Healthy volunteers: Yes
Phase: PHASE4
Enrollment: 100
Sponsor: Brigham and Women's Hospital

Location: Brigham and Women's Hospital Boston Massachusetts

Summary

The central objective of this study will be to evaluate the relationship between estrogen levels and the pain following oocyte retrieval in women undergoing in vitro fertilization.

Eligibility Criteria

Inclusion Criteria: * American Society of Anesthesiologists (ASA) I to III health status (moderate systemic disease), * Age between 18 and 50 yrs * Undergoing oocyte retrieval with intravenous general anesthesia. Exclusion Criteria: * Refuse or withdraw their consent * Fail to adequately respond to IVF stimulations medications, and thus are not eligible for oocyte retrieval.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT03105518). StuddyBuddy aggregates publicly available trial information.