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Comparison of the effects of planar nerve block of the erector spinae and transversus abdominis on the recovery of gastrointestinal function after laparoscopic sleeve gastrectomy in patients with laparoscopic sleeve gastrectomy

Comparison of the effects of planar nerve block of the erector spinae and transversus abdominis on the recovery of gastrointestinal function after laparoscopic sleeve gastrectomy in patients with laparoscopic sleeve gastrectomy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085920
Enrollment
Unknown
Registered
2024-06-21
Start date
2024-06-21
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

Postoperative gastrointestinal dysfunction

Interventions

Ultrasound-guided erector spinae plane block group:Before induction of anesthesia, an ultrasound-guided planar block of the erector spinae muscle was performed in the patients T8 plane bilaterally wit

Sponsors

Suqian First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients must meet all of the following inclusion criteria to be enrolled in this study 1) Patients who underwent elective laparoscopic sleeve gastrectomy; 2) Age 18 to 60 years; 3) American Society of Anesthesiologists (ASA) classification of II to III; 4) Morbidly obese patients; (5) Patients who voluntarily participated in this study and signed the relevant informed consent form.

Exclusion criteria

Exclusion criteria: Patients with any of the following are not eligible for enrollment in this study 1) Patients with a history of mental illness, alcoholism, drug abuse, or chronic pain; 2) Patients with severe cardiac, hepatic and renal dysfunction; 3) Patients with a history of previous gastrointestinal surgery; 4) Patients who are allergic to intraoperative related drugs; 5) other conditions that the investigator considers inappropriate for participation in this trial.

Design outcomes

Primary

MeasureTime frame
Time to first postoperative bowel movement;Postoperative I-FEED score (postoperative day 3);

Secondary

MeasureTime frame
Postoperative nausea and vomiting VAS score;Postoperative pain NRS score;Quality of Recovery QoR-15 rating;SII (Systemic Immunoinflammatory Index) and NLR and PLR preoperatively, on the first postoperative day and on the third postoperative day;;Postoperative anesthesia and surgery-related complications;

Countries

China

Contacts

Public ContactJingying Liu

Suqian First People's Hospital

434422658@qq.com+86 188 0060 8517

Outcome results

None listed

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