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NCT06929000Recruiting

A Study on Application of Adjustable Headrest in Painless Curettage Surgery for Overweight and Obese Patients

A Study on Application of Adjustable Headrest in Painless Curettage Surgery for Overweight and Obese Patients: a Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 15 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of this study is to observe the effect of adjustable headrests on ventilation function in overweight and obese patients through clinical experiments, and to explore the impact on the incidence of hypoxemia during painless curettage in overweight and obese patients. Participants will be randomly allocated to three groups: the supine head-straight position group(Group A), the supine head-lateral position group(Group B), and the adjustable headrest group(Group C). These three groups of patients underwent painless curettage surgery in the daytime operating room and the occurrence of hypoxemia will be observed.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
300 (estimated)
First submitted
27 Mar 2025
Start date
25 Feb 2025
Primary completion date
22 Feb 2026
Lead sponsor
Maternal and Child Health Hospital of Hubei Province
Diseases
Obesity
NCT number
NCT06929000

What you commit to

  • Study type: Interventional
  • Planned participants: 300
  • From 25 Feb 2025 to the primary completion date, 22 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Abnormal lung function or respiratory system diseases
  • psychiatric disorders

Other

  • Airway obstruction or respiratory malformation
  • cervical spondylosis

Who the study is looking for

  • patients who choose to have painless surgical abortion
  • Body mass index greater than 24
  • the American Society of Anesthesiologists (ASA) physical status ranked I-II
  • competent to provide informed consent

Age in the registry: 20 years to 50 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Maternal and Child Health Hospital of Hubei Province,
Coordinator of this site? Confirm its status
WuhanChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.