Menstrual Status, Anesthetic Consumption, and PONV

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-65
SponsorAnkara Etlik City Hospital

About this trial

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 criteria

Qualifiers

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

Disqualifiers

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)

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

120 Participants
are grouped into 3 trial groups

Sponsors and collaborators