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Effects of different pneumoperitoneum pressures on perioperative atelectasis assessed by lung ultrasonography during robot-assisted gynaecological surgery: a prospective, randomised controlled trial

Effects of different pneumoperitoneum pressures on perioperative atelectasis assessed by lung ultrasonography during robot-assisted gynaecological surgery: a prospective, randomised controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085515
Enrollment
Unknown
Registered
2024-06-11
Start date
2024-06-14
Completion date
Unknown
Last updated
2024-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perioperative atelectasis

Interventions

Low pneumoperitoneum pressure (LPP) group:Pneumoperitoneum pressure was set to 12 mmHg.
Standard pneumoperitoneum pressure (SPP) group:Pneumoperitoneum pressure was set to 15 mmHg.

Sponsors

Obstetrics and Gynecology Hospital, School of Medicine, Tongji University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Women aged 20 to 80 years, and of American Society of Anesthesiologists’(ASA) physical status 1 or 2, undergoing elective robot-assisted gynaecological surgery were eligible for inclusion.

Exclusion criteria

Exclusion criteria: The exclusion criteria included patient refusal, BMI more than 35kg·m-2, moderate/severe chronic obstructive pulmonary disease (forced expiratory volume in 1 s <30% of the predicted value), cardiac or neuromuscular diseases, previous intrathoracic procedure, and any contraindication to radial artery cannulation.The following patients were also excluded: (1) those with preoperative ultrasound evidence of pulmonary atelectasis; (2) those undergoing conversion from laparoscopic to open surgery; and (3) those experiencing critical postoperative pulmonary complications such as severe respiratory infection and pneumothorax. .

Design outcomes

Primary

MeasureTime frame
Modified lung ultrasound score;

Secondary

MeasureTime frame
the appearance of recruitment manoeuvres after surgery; intraoperative and postoperative incidences of desaturation;PACU residence time;PaO2/FIO2;

Countries

China

Contacts

Public ContactRong Lin

Obstetrics and Gynecology Hospital, School of Medicine, Tongji University

linrong@51mch.com+86 189 3087 1310

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026