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Effect of Low-Pressure Pneumoperitoneum Combined with Deep Neuromuscular Block on Postoperative Recovery in Patients Undergoing Laparoscopic Bariatric Surgery

Low-pressure pneumoperitoneum combined with deep neuromuscular block anesthesia for postoperative recovery in patients undergoing laparoscopic sleeve gastrectomy: a single-center randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117032
Enrollment
Unknown
Registered
2026-01-19
Start date
2026-01-19
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Obesity and related metabolic diseases

Interventions

Experimental Group:Low-pressure pneumoperitoneum (8 mmHg) combined with deep neuromuscular block (target TOF=0, PTC=1-2)
Control Group:Standard-pressure pneumoperitoneum (13 mmHg) combined with moderate neuromuscular block (target TOF count 1-3)

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Patients who present to the Bariatric Center from 2026 to 2028, meet the indications for metabolic surgery, and are scheduled to undergo laparoscopic sleeve gastrectomy. (2) Body mass index (BMI) between 27.5 kg/m² and 45 kg/m², inclusive. (3) Age between 16 and 70 years, inclusive.

Exclusion criteria

Exclusion criteria: (1)Patients with BMI >45 kg/m² or BMI 40) requiring non-invasive ventilation or oxygen therapy before surgery. (10) Patients who actively decline to participate in the trial. (11) Patients using medications known to interact with rocuronium preoperatively (including aminoglycosides, lincosamides, polypeptides, acylaminopenicillins, tetracyclines, metronidazole, phenytoin and carbamazepine, diuretics, monoamine oxidase inhibitors, calcium channel blockers, magnesium agents). (12) Patients lost to follow-up.

Design outcomes

Primary

MeasureTime frame
Index of Nausea, Vomiting, and Retching (INVR) score on postoperative day;

Secondary

MeasureTime frame
Operative time;Postoperative quality of recovery (Quality of Recovery-40, QoR-40 score);Postoperative pain score (Visual Analogue Scale, VAS);Postoperative serum inflammatory markers (C-reactive protein, CRP; Interleukin-6, IL-6);Postoperative complications (Clavien-Dindo classification);Nausea and vomiting score on postoperative day 3 (INVR score on POD3);

Countries

China

Contacts

Public ContactPurun Lei

The Third Affiliated Hospital of Sun Yat-sen University

leipurun@163.com+86 186 2012 1924

Outcome results

None listed

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