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The Analgesic Efficacy of Transverse Abdominal Plane Block for Laparoscopic Surgery among Japanese Patients: a Randomized Controlled Trial.

The Analgesic Efficacy of Transverse Abdominal Plane Block for Laparoscopic Surgery among Japanese Patients: a Randomized Controlled Trial. - Transverse Abdominal Plane Block for Laparoscopic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002664
Enrollment
50
Registered
2009-10-24
Start date
2009-10-01
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

Cholecystitis, Ovarian cyst

Interventions

TAP block group: after induction of standard general anesthesia, echo-guided TAP block will be performed. The anesthesiologist who performs TAP block will be different from the one who inducts and mai
postoperative pain, symptoms, and analgesic dose will be different from the anesthesiologist who inducts and maintains general anesthesia, and the TAP blocker. Duration of Intervention
From October 21, 2009 to December 31, 2009. Control group: Same preparation of TAP block will be proceeded (disinfection of abdominal skin, abdominal description by echography, etc.) after eve
postoperative pain, symptoms, and analgesic dose will be different from the anesthesiologist who inducts and maintains general anesthesia, and the TAP blocker.

Sponsors

St. Luke's International Hospital
Lead Sponsor
Center for Clinical Epidemiology, St. Luke&#39
Collaborator
s Life Science Institute
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: # Patients undergoing laparoscopic cholecystectomy, ovarian cystectomy, and salpingo-oophorectomy # Scheduled surgery # Patients whose physical status classification of America Society of Anesthesiologists (ASA) is 1 or 2. # Those who gives written informed consent.

Exclusion criteria

Exclusion criteria: # Those who have allergic history against local anesthetic drugs (amide type) # The cases that are converted to open surgery. # Those who are prescribed narcotic analgesics or NSAIDs preoperatively.

Design outcomes

Primary

MeasureTime frame
#Postoperative pain at 30min and 24 hours after surgery using Numerical Rating Scale (NRS). #Intra- and postoperative dose of narcotic analgesics, #Time from surgery to first analgesics use. # Postoperative dose of NSAIDs and acetaminophen. #Postoperative symptoms (nausea, vomiting)

Countries

Japan

Outcome results

None listed

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