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A randomized non-inferiority controlled trial of postoperative analgesic effect of epidural anesthesia and rectus sheath block in laparoscopic surgery

A randomized non-inferiority controlled trial of postoperative analgesic effect of epidural anesthesia and rectus sheath block in laparoscopic surgery - A randomized non-inferiority controlled trial of postoperative analgesic effect of epidural anesthesia and rectus sheath block in laparoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038104
Enrollment
80
Registered
2019-09-26
Start date
2019-10-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients who received either laparoscopic gastrectomy or laparoscopic colectomy.

Interventions

Epidural anesthesia group Before inducing anesthesia, perform catheter placement at the 9th to 11th thoracic vertebrae levels. Administer 0.375% ropivacaine epidurally at the start of wound closur

Sponsors

University of Tsukuba
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients scheduled to undergo laparoscopic gastrectomy or laparoscopic colorectal resection of 6 cm or less where the wound is continuous with the umbilicus in addition to the port hole. Age: 20 years old and younger than 80 years old at the time of obtaining consent ASA-PS (American Society of Anesthesiologists physical status): 1-3 Patients who have received sufficient explanation for participation in this study, and who have fully understood and agreed to the document by their own will.

Exclusion criteria

Exclusion criteria: Antiplatelet / anticoagulant therapy There is a decrease in platelet count (80,000 <mcL), blood coagulation ability abnormality (aPTT> control value + 10 seconds or PT (%) <50%) History of spine surgery There is an allergy to the anesthetic used Weight less than 40 kg BMI> 30 kg / m2 Patients whose pain is difficult to evaluate (psycho-neuropathy, dementia, restlessness, etc.) Use regular painkillers Liver dysfunction (AST or ALT> 100 IU / L) Renal dysfunction (eGFR <50 mL / min / 1.73m2)

Design outcomes

Primary

MeasureTime frame
Pain scale (Numerical Rating Scale) when coughing 24 hours after surgery

Countries

Japan

Contacts

Public ContactYohei Owada

University of Tsukuba Department of Gastrointestinal and Hepato-Biliary-Pancreatic Surgery

y.owada@md.tsukuba.ac.jp029-853-3221

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026