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Effectiveness and Duration of Postoperative analgesia with 5% Lignocaine patch in Patients Receiving Transversus Abdominis Plane Block in Laparoscopic Abdominal Surgeries

Effectiveness and Duration of Postoperative analgesia with 5 percentage Lignocaine patch in Patients Receiving Transversus Abdominis Plane Block in Laparoscopic Abdominal Surgeries - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099037
Enrollment
68
Registered
2025-12-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Nil: Nil Intervention2: 5 percentage Lignocaine patch: transdermal lignocaine patch will be applied over the surgical trocar site after admistering TAP block post laproscopic abdominal

Sponsors

KS Hegde Medical Academy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age: 18 60 years 2. ASA physical status I or II 3. Undergoing elective laparoscopic abdominal surgery 4. Informed consent obtained

Exclusion criteria

Exclusion criteria: 1. Allergy to local anesthetics 2. Chronic pain conditions or regular analgesic use 3. Skin lesions or infections at patch application site 4. Laproscopic surgeries converted to open 5. Upper abdominal laparoscopic surgeries

Design outcomes

Primary

MeasureTime frame
To compare postoperative duration duration of postoperative analgesia between patients receiving a TAP block with a topical 5% lidocaine patch versus TAP block alone in patients undergoing laparoscopic abdominal surgery.Timepoint: Postoperative pain intensity will be assessed at 12, 24, and 48 hours postoperatively using validated standard pain assessment tools.

Secondary

MeasureTime frame
To assess the time to first request for rescue analgesia postoperatively in both groups. To compare total opioid consumption post-surgery. To evaluate the incidence & severity of breakthrough pain after the effect of TAP block diminishes. To compare time to first ambulation & early functional recovery.Timepoint: To assess time to first request for rescue analgesia within 48 hours postoperatively. To compare total opioid consumption during the first 24 & 48 hours after surgery. To evaluate breakthrough pain at 12 24 & 48 hours postoperatively. To compare time to first ambulation & early functional recovery within 24 hours after surgery.

Countries

India

Contacts

Public ContactDR AVANISH BHANDARY

K.S Hegde Medical Academy

avanishbhandary@gmail.com9845679949

Outcome results

None listed

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