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Comparison between ultrasound guided modified thoracoabdominal perichondrial approach nerve block versus oblique subcostal transverse abdominis plane block.

To compare the postoperative analgesia between ultrasound guided modified thoracoabdominal nerve block through perichondrial approach versus oblique subcostal transabdominal plane block for patients undergoing laparoscopic cholecystectomy: a randomised study. - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078005
Enrollment
186
Registered
2024-12-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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: POSTOPERATIVE ANALGESIC NERVE BLOCKS: ropivacaine 0.2% Intervention2: USG guided modified thoracoabdominal perichondrial approach nerve block: 25 ml of ropivacaine 0.2% injected bilater

Sponsors

Dr SOHAIL HASAN LASKAR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients in the American Society of Anaesthesiologists (ASA) grading I and II Patients posted for elective laparoscopic cholecystectomy under general anaesthesia. Availability of informed and written consent from the patient party.

Exclusion criteria

Exclusion criteria: BMI more than 35 kg per m² at the time of the surgery. Patient weighing less than 34kg at the time of surgery. History of allergy to any local anaesthetic. Patients having coagulopathy or bleeding disorder are to be excluded. Patients having infection at the site of block are to be excluded. Patients having neurological deficits or on analgesic for chronic pain. Patients having neuropsychiatric disorders hearing impairment.

Design outcomes

Primary

MeasureTime frame
To compare the duration of analgesia between the two groups in the first 24 postoperative hours.Timepoint: To compare the duration of analgesia between the two groups at 0 min, at 15 mins, at 30 mins, at 60 mins, at 6 hours, at 12 hours and at 24 hours time intervals.

Secondary

MeasureTime frame
1. To compare the total analgesic requirements between the two groups in the first 24 postoperative hours. Timepoint: Within 24 hours.;To compare the NRS pain scores between two groups at rest & at motion.Timepoint: At 0 min, at 15 mins, at 30 mins, at 60 mins, at 6 hours, at 12 hour and at 24 hours. ;Presence of post-operative shoulder pain postoperatively. (Yes/No)Timepoint: Within 24 hours.

Countries

India

Contacts

Public ContactDr Sohail Hasan Laskar

Gauhati medical college and hospital

faizaahmedtalukdar@gmail.com9864031429

Outcome results

None listed

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