Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Ultrasound-guided lung recruitment to prevent postoperative lung complications after total laparoscopic hysterectomy in people with obstructive sleep apnea

Official title: Effects of Ultrasound-guided Recruitment Manoeuvres on Postoperative Pulmonary Complications in OSA Patients Undergoing Total Laparoscopic Hysterectomy

Run by The First Affiliated Hospital of Xinxiang Medical College · NCT07362680 · Data updated 2026-11-12

This trial will test whether ultrasound-guided lung recruitment maneuvers can reduce postoperative pulmonary complications in adults with obstructive sleep apnea having total laparoscopic hysterectomy.

More Laparoscopic Hysterectomy trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment90 (estimated)
SponsorThe First Affiliated Hospital of Xinxiang Medical College
Academic / other
Locations1 site (Xinxiang, Henan)
StatusRecruiting
StartedMay 2, 2025
Main results expectedAugust 31, 2026
Study endsAugust 31, 2026
Registry record updatedJanuary 23, 2026
Trial IDNCT07362680 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18 years) with BMI >28 kg/m², STOP-BANG score ≥3, ASA I–III who are scheduled for elective total laparoscopic hysterectomy are the intended participants.

Probably not a fit

Patients with pre-existing severe pulmonary disease, abnormal preoperative chest imaging, severe cardiac arrhythmias, prior cardiac surgery, or allergies to study medications are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Adults with obstructive sleep apnea who meet BMI and STOP-BANG criteria and are scheduled for elective total laparoscopic hysterectomy will receive one of three intraoperative lung recruitment strategies: sustained inflation, incremental PEEP, or ultrasound-guided recruitment. Investigators will compare postoperative pulmonary complications, including atelectasis, and will use end-expiratory lung volume (EELV) measurements to judge how effectively each maneuver re-expands the lung. The ultrasound-guided arm uses bedside lung ultrasound to guide recruitment delivery and to detect residual consolidation. The protocol focuses on short-term respiratory outcomes and the practicality of using EELV as an effectiveness metric.

Why it matters

Potential benefit: If successful, ultrasound-guided recruitment could reduce postoperative atelectasis and other lung complications, improving breathing recovery after laparoscopic hysterectomy in OSA patients.

How similar studies have gone: Recruitment maneuvers have reduced atelectasis and improved oxygenation in other surgical populations, but ultrasound-guided recruitment with EELV monitoring is relatively novel for OSA patients undergoing laparoscopic hysterectomy.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥ 18 years;
* Scheduled for elective total laparoscopic hysterectomy;
* American Society of Anesthesiologists (ASA) I to III;
* BMI \> 28 kg/m²;
* STOP-BANG score ≥ 3.

Exclusion Criteria:

* Abnormal findings on preoperative chest X-ray or CT, such as atelectasis, pneumothorax, thoracic deformity, pleural effusion, or neuromuscular diseases;
* Pre-existing severe pulmonary diseases;
* Severe cardiac arrhythmias or a history of cardiac surgery;
* Allergy to any medications used in the study.

Where it's running

  • The First Affiliated Hospital of Xinxiang Medical College
    Xinxiang, Henan, China
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.