Skip to content

Comparison between transverse abdominal block and quadratus lumborum block in patients undergoing laparoscopic intraperitoneal onlay mesh repair in umbilical hernia in adults.

A Comparative evaluation between Transverse abdominal plane block versus Quadratus lumborum block in intraperitoneal onlay laparoscopic umbilical hernia mesh repair in adults:A Prospective randomised controlled study. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068266
Enrollment
40
Registered
2024-06-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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: Transverse abdominis plane block in intraperitoneal onlay laproscopic umbilical hernia mesh repair in adults.: Patients undergoing intra peritoneal onlay laparoscopic umbilical hernia m

Sponsors

Dr Alieshia Siangshai
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA grade 1 and 2 patients. 2. Patients undergoing umbilical hernia repair under general anaesthesia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
To compare the duration of postoperative analgesia using Injection Levobupivacaine 0.25% 20ml on each side by TAP block and QL block in patients undergoing intraperitoneal onlay laparascopic umbilical hernia repair in adults.Timepoint: To compare the duration of postoperative analgesia using Injection Levobupivacaine 0.25% 20ml on each side by TAP block and QL block in patients undergoing intraperitoneal onlay laparascopic umbilical hernia repair in adults at 2hours,4 hours, 8 hours,12 hours and 24 hours.

Secondary

MeasureTime frame
1.Hemodynamic parameters like NIBP,HR, BP and Spo2 for 24 hours postoperatively. 2.Post operative Visual Analogue Scale pain score. 3. Time of rescue analgesia. 4. Adverse effects.Timepoint: First 24 hours monitoring.

Countries

India

Contacts

Public ContactDr Karthik G S

Raja Rajeshwari medical college and hospital

drgskarthik@gmail.com9538220515

Outcome results

None listed

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