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Comparison of the effects of incision-based multi-point rectus sheath block and bilateral rectus sheath block in laparoscopic radical gastrectomy for gastric and colorectal cancer

Comparison of the effects of incision-based multi-point rectus sheath block and bilateral rectus sheath block in laparoscopic radical gastrectomy for gastric and colorectal cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083821
Enrollment
Unknown
Registered
2024-05-06
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Patients undergoing Laparoscopic radical gastrectomy for gastric or colonic cancer

Interventions

Group IBRSB:Incision based multi-point RSB
Group RSB:Bilateral RSB

Sponsors

the First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective laparoscopic radical resection of gastric or colorectal cancer; signed informed consent; age 18-75 years old; ASA grade I and III; BMI 18~30 kg/?

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to the regional block technique (allergy to local anesthetics, infection around the puncture site, and coagulation disorders); 2. History of dependence on painkillers and alcoholism; 3. Dementia or severe cognitive impairment; 4. Any cerebrovascular accident occurred within 3 months, such as stroke, transient ischemic attack (TIA); 5. Patients with severe hypertension or unstable preoperative blood pressure control; 6. The operation was cancelled for various reasons; 7. Anyone who has trouble communicating.

Design outcomes

Primary

MeasureTime frame
Intraoperative dosage of remifentanil;

Secondary

MeasureTime frame
Resting, coughing pain scores;Dosage of other anesthetic drugs during surgery; Intraoperative blood pressure, heart rate;First postoperative relief analgesia time;Postoperative remedial analgesic drug dosage;Dosage of analgesic pump used 24 and 48 hours after surgery;Opioid side effects (nausea and vomiting, dizziness, pruritus, sleepiness, respiratory depression,etc);Time to ambulation;Exhaust time;Time to get out of bed;Surgery duration;Hospital stay duration;Total hospitalization expenses;

Countries

China

Contacts

Public ContactGuanghong Xu

Department of Anesthesiology, the First Affiliated Hospital of Anhui Medical University

xuguanghong2004@163.com+86 138 5694 9535

Outcome results

None listed

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