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Prospective study of postoperative analgesia with or without epidural anesthesia in laparoscopic colectomy

Prospective study of postoperative analgesia with or without epidural anesthesia in laparoscopic colectomy - Prospective study of postoperative analgesia with or without epidural anesthesia in LAC

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000040756
Enrollment
200
Registered
2020-06-14
Start date
2020-07-01
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

colorectal cancer

Interventions

None listed

Sponsors

Kanagawa Cancer Center Department of Gastrointestinal Surgery
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Histologically confirmed colorectal cancer 2)Laparoscopic primary tumor resection 3)No simultaneous resection, but ostomy is acceptable 4)Adequate organ function as evidenced by the following laboratory studies within 28 days prior to enrollment; PLT >= 80,000 /mm3 PT-INR =< 1.1 APTT =<39 sec 5)Age:>=20 years old 6)Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 7) Appropriate answers to questionnaires 8) Written informed consent

Exclusion criteria

Exclusion criteria: 1) Emergency surgery 2) Use of anticoagulants and antiplatelet drugs 3) Severe drug hypersensitivity 4) Women during pregnancy or possible pregnancy 5) Other conditions judged ineligible by physician

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS) pain score 7 days after surgery

Secondary

MeasureTime frame
Minimum value of VAS scale 7 days after surgery Time from entering the operating room to the start of surgery Incidence of postoperative complications Time until first walking and exhaust gas after surgery

Countries

Japan

Contacts

Public ContactAya Kato

Kanagawa Cancer Center Department of Gastrointestinal Surgery

kato_12th@yahoo.co.jp045-520-2222

Outcome results

None listed

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