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Effect of Intra-Operative Infusion of Lidocaine Versus Ultrasound-Guided Transverse Abdominal Plane Block on Postoperative pain and Bowel function Recovery in Patients Undergoing Laparoscopic cholecystectomy

Effect of Intra-Operative Infusion of Lidocaine Versus Ultrasound-Guided Transverse Abdominal Plane Block on Postoperative pain and Bowel function Recovery in Patients Undergoing Laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250412002
Enrollment
100
Registered
2025-04-12
Start date
2022-12-10
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

The study focused on the following health conditions: laparoscopic cholecystectomy ,Postoperative Pain TAP block - laparoscopic cholecystectomy (LC)- lidocaine infusion - postoperative recovery-postoperative pain.

Interventions

After general anesthesia, a bilateral TAP block was performed usingultrasound guidance. A 22G sterile puncture needle was used toinject 20 ml of isobaric Marcaine 0.25% into the triangle of Petit,loca
Active Comparator Drug,Active Comparator Drug
Transversus Abdominis Plane (TAP) Block,Intravenous Lidocaine Infusion (LID)

Sponsors

None listed

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Adult Patients: Individuals aged 21 to 60 years. Scheduled forElective Laparoscopic Cholecystectomy. 2. Patients set to undergo this specific surgical procedure. ASAPhysical Status I and II: Patients classified as having low to moderate anesthesia risk. Absence of CertainConditions:

Exclusion criteria

Exclusion criteria: Acute Cholecystitis: Patients diagnosed with this condition. 1.History of Acute Pancreatitis: . 2.Liver Cirrhosis: Patients suffering from this liver disease. 3.Associated Common Bile Duct Stones: Individuals with stones in the common bile duct. 4. Converted to Open Cholecystectomy: Patients who had their laparoscopic procedure changed to an open surgery.

Design outcomes

Primary

MeasureTime frame
Pain Level 4, 6, 12, and 24 hours post-surgery Visual Analog Scale (VAS) (0-10)

Secondary

MeasureTime frame
Postoperative Bowel Recovery Post-surgery Time to first bowel movement (hours)

Countries

Egypt

Contacts

Public ContactAmira Abo Elnasr Aw

Department of Anesthesiology,Intensive care & painmanagement, Faculty ofMedicine for Girls, Al-AzharUniversity.

AMIRAABOELNASR.MEDG@AZHAR.EDU.EG01006739558

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026