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Ultrasounn guided peripheral nerve block with local anaesthetics for postoperative analgesia in laparoscopic abdominal suergeries

Ultrasound Guided Trans versus Abdominis Plane Block With Levobupivacaine And Ropivacaine For Postoperative Analgesia In Laproscopic Abdominal Surgeries Under General Anesthesia In Tertiary Care Hospital:A Comparative Study - nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079528
Enrollment
60
Registered
2025-01-27
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: K358- Other and unspecified acute appendicitis Health Condition 2: Z302- Encounter for sterilization

Interventions

Intervention1: Ultrasound Guided Transversus Abdominis Plane Block: Ultrasound Guided Transversus Abdominis Plane Block with Levobupivacaine for post operative analgesia Control Intervention1: Ultraso

Sponsors

GAYATRI VIDYA PARISHAD INSTITUTE OF HEALTH CARE AND MEDICAL TECHNOLOGY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients taken for surgeries: elective abdominal laparoscopic surgeries (laparoscopic tubectomies, cystectomies, appendectomies, hernioplasty) under general anaesthesia.

Exclusion criteria

Exclusion criteria: Patients who are allergic to study drugs. Patients having severe cardiac, pulmonary and renal diseases. Patients in whom abdominal drain is kept. Patients who are unwilling to participate in the study. Pregnant and lactating women. Patients who do not satisfy inclusion criteria Patients with coagulopathy. Patients who are unable to give informed consent. Patients who cannot understand VAS score. Patients who are converted to open surgery

Design outcomes

Primary

MeasureTime frame
Magnitude of pain assessed by visual analogue score (VAS).Timepoint: 30minutes, 1st, 2nd, 4th, 6th, 8th,12th,24 hours post surgery

Secondary

MeasureTime frame
Time to first analgesia request.Timepoint: first 24 hours post surgery;Adverse effects like bradycardia, hypotension, nausea, vomiting and respiratory depressionTimepoint: first 24hours post surgery;analgesic requirementTimepoint: first 24hours post surgery;patient satistfactionTimepoint: 24 hours post surgery

Countries

India

Contacts

Public Contactthottikat kaarthika

GAYATRI VIDYA PARISHAD INSTITUTE OF HEALTH CARE AND MEDICAL TECHNOLOGY

karthika.mohan07@gmail.com9908888134

Outcome results

None listed

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