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Evaluation of pulmonary complications during laparoscopic surgery in patients with protective mechanical ventilation combined deep neuromuscular block

Effects of protective pulmonary ventilation combined deep neuromuscular block during general anesthesia in colorectal laparoscopic surgery on postoperative pulmonary complications, lung injury, pain and inflammatory response

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054215
Enrollment
Unknown
Registered
2021-12-11
Start date
2023-01-01
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Colorectal cancer

Interventions

Group 1:Lung-protective ventilation combined with deep neuromuscular blockade and low pneumoperitoneum pressure
Group 2:Conventional pulmonary ventilation combined with moderate NMB (neuromuscular blockade) and conventional pneumoperitoneum pressure

Sponsors

National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Male and female patients aged between 18 and 80 years old; 2. American Society of Anesthesiologists (ASA) physical status 44 defines as high risk).

Exclusion criteria

Exclusion criteria: 1. Pregnant or breast-feeding status; 2. Had a history of recent pulmonary infection or diagnosis of pneumothorax, giant bullae, chronic obstructive pulmonary disease; 3. Diagnosis of severe cerebral and cardiovascular dysfunction; 4. Diagnosis of chronic renal failure with dialysis; 5. Diagnosis of hepatic dysfunction (Child-Pugh grade B or C); 6. Diagnosis of immunologic or neuromuscular disease; 7. Had a history of prior lung or abdominal surgery; 8. Emergency or unplanned surgery; 9. Expected prolonged mechanical ventilation after surgery; 10. Allergies or contraindications to sevoflurane, propofol, or nonsteroidal anti-inflammatory drugs (NSAIDs); 11. Participated in other drug trials within 1 preoperative month.

Design outcomes

Primary

MeasureTime frame
Postoperative Pulmonary Complications;

Secondary

MeasureTime frame
Neutrophil Elastase, NE;Angiopoietin, ANG2;Clara cell secretory protein, CC16;Modified Clinical Pulmonary Infection Score, mCPIS;Postoperative pulmonary complications, PPCs;Surgical rating scale, SRS;White blood cell, WBC;Neutrophils;Lymphocyte;C-reactive protein;Nuclear factor kappa-B, NF-?B;Tumor Necrosis Factor-a, TNF-a;IL-1ß;IL-6;Intraoperative ventilation index;Acute pain numerical rating scale;Chronic pain numerical rating scale;Post-operative pain when nausea/vomiting;Soluble receptor for advanced glycation end-products, sRAGE;

Countries

China

Contacts

Public ContactYan Tao

National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

blizzardyt@163.com+86 13522553375

Outcome results

None listed

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