RecruitingNCT07456202

Menstrual Status, Anesthetic Consumption, and PONV

Impact of Menstrual Phases and Menopause on Intraoperative Anesthetic Consumption and Postoperative Nausea and Vomiting: A Prospective Observational Study


Sponsor

Ankara Etlik City Hospital

Enrollment

120 participants

Start Date

Mar 7, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

This prospective observational cohort study aims to evaluate the association between menstrual phase (determined by postoperative serum progesterone levels), intraoperative anesthetic consumption, and the incidence and severity of postoperative nausea and vomiting (PONV) in female patients undergoing cholecystectomy. Intraoperative anesthetic requirements will be recorded, and postoperative nausea and vomiting will be assessed using standardized scoring systems.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 65 Years

Inclusion Criteria4

  • Female patients aged 18 to 65 years
  • American Society of Anesthesiologists (ASA) physical status I-II-III
  • Scheduled for elective laparoscopic cholecystectomy under general anesthesia
  • Willing and able to provide written informed consent

Exclusion Criteria16

  • Age outside the specified range (younger than 18 or older than 65 years)
  • Male patients
  • American Society of Anesthesiologists (ASA) physical status ≥ IV
  • Severe systemic comorbidities (e.g., significant cardiovascular, hepatic, renal, or pulmonary disease)
  • Conversion from laparoscopic to open cholecystectomy
  • History of alcohol, drug, or substance abuse
  • Visual or hearing impairment interfering with study assessments
  • Current hormone replacement therapy
  • Use of oral contraceptives
  • Preoperative nausea or vomiting
  • History of severe postoperative nausea and vomiting
  • Neurological or psychiatric disorders affecting assessment reliability
  • Hemodynamic instability during surgery
  • Postoperative admission to intensive care unit
  • Acute cholecystitis at the time of surgery
  • Refusal to participate or inability to provide informed consent

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

Ankara Etlik City Hospital

Ankara, Ankara, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07456202


Related Trials