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EFFECTIVENESS OF BILATERAL TRANSVERSUS ABDOMINIS PLANE BLOCK WITH LINEA SEMILUNAR APPROACH COMPARED TO LATERAL APPROACH AS ANALGESIA TECHNIQUE FOR COLORECTAL SURGERY

EFFECTIVENESS OF BILATERAL TRANSVERSUS ABDOMINIS PLANE BLOCK WITH LINEA SEMILUNAR APPROACH COMPARED TO LATERAL APPROACH AS ANALGESIA TECHNIQUE FOR COLORECTAL SURGERY : A single blinded randomized controlled trial

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240918009
Enrollment
40
Registered
2024-09-18
Start date
2024-08-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

colorectal surgeries transversus abdominis plane block Colorectal Surgery transversus abdominis regional anesthesia

Interventions

local anesthestic will be deposited to the transversus abdominis plane. in the lateral approach, 20 ml of 0.25% bupivacain will be injected to the desired location (transversus abdominis plane) at eac
Experimental Procedure/Surgery,Experimental Procedure/Surgery
transversus abdominis plane block with lateral approach,transversus abdominis plane block with semilunar approach

Sponsors

Anesthesiology and intensive therapy department, faculty of medicine, Udayana University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. patient between 18 to 65 year old 2. body mass index between 17.5 to 25 kg/m2 3. ASA Physical status classification I to III

Exclusion criteria

Exclusion criteria: 1. body mass index less than 17.5 kg/m2 or more than 25 kg/m2 2. ASA Physical status classification IV and above 3. History of allergy to the investigational drug 4. Infection signs in the respective investigational site 5. Severe Cardiovascular impairment 6. Chronic opioid consumption 7. Consumption of blood thinner or antiplatelets which causes coagulopathy during the surgery. 8. subject or guardian refusal to participate in the study 9. subjects with consciousness impairment

Design outcomes

Primary

MeasureTime frame
Analgesia duration After surgery, time to first analgesia dose Hours

Secondary

MeasureTime frame
Pain score 1,6, 12, 24 and 48 hours after surgery Visual Analog Scale,Opioid (morphine) consumption 24 and 48 hours after surgery mg,Quality of recovery 24 and 48 hours after surgery Quality of recovery 40 questionairre

Countries

Indonesia

Contacts

Public ContactKadek Adwitya

Anesthesiology and intensive therapy department, faculty of medicine, Udayana University

kadekindriani@student.unud.ac.id0812383790

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026