Actively Recruiting

Age: 18Years - 40Years
FEMALE
NCT07242209

Sugammadex and Menstrual Cycle in Postoperative Nausea and Vomiting

Led by Sakarya University · Updated on 2026-03-10

60

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This observational study aims to evaluate the relationship between menstrual cycle phases and the incidence of postoperative nausea and vomiting (PONV) in women of reproductive age undergoing septorhinoplasty surgery. The study's primary objective is to determine whether different phases of the menstrual cycle are associated with variations in PONV frequency. As a secondary objective, the relationship between menstrual phases, PONV incidence, and the use of sugammadex during anesthesia will be analyzed. No additional intervention will be applied beyond routine clinical practice; all data will be collected prospectively from anesthesia records and postoperative evaluations.

CONDITIONS

Official Title

Sugammadex and Menstrual Cycle in Postoperative Nausea and Vomiting

Who Can Participate

Age: 18Years - 40Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female sex
  • Age between 18 and 40 years
  • Regular menstrual cycle
  • Scheduled for ENT (ear, nose, and throat) surgery
  • Classified as ASA physical status I or II
Not Eligible

You will not qualify if you...

  • Irregular menstrual cycle
  • Unknown date of last menstrual period
  • Receiving estrogen and/or progesterone supplementation
  • Pre-menopausal or menopausal status
  • Pregnant
  • Breastfeeding
  • Classified as ASA physical status III or IV
  • Apfel score 63 3
  • History of drug allergy
  • Surgery duration exceeding 3 hours
  • Age <18 or >40 years

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sakarya University-Anesthesiology and Reanimation Department

Sakarya, Serdivan, Turkey (Türkiye), 54050

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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