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To assess the efficacy of dexmedetomidine and levobupivacaine in tap block for Post operative pain

A comparative evaluation of Efficacy of 0.5% levobupivacaine Versus 0.5% levobupivacaine with dexmedetomidine in Ultrasound guided transversus abdominis plane block for Post operative analgesia in patients undergoing abdominal surgeries - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055537
Enrollment
60
Registered
2023-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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 abdominus plane block in abdomen surgery: A Comparative evaluation of Efficacy of 0.5% levobupivacaine Versus 0.5% levobupivacaine with dexmedetomidine in Ultrasound guided t

Sponsors

Career institute of medical science and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I/II belonging to American Society of Anaesthesiologists (ASA) Age group 18 to 65 years Patient undergoing abdominal surgeries under general anesthesia/spinal anesthesia will enrolled in the study Patient willing to give consent

Exclusion criteria

Exclusion criteria: Patients with history of : Allergy to LEVOBUPIVACAINE Body mass index >35 kg.mâ??2 Preoperative opioid or nonsteroidal anti-inflammatory drug treatment for chronic pain. Morbid obesity Cardiac disorders - ischaemic heart disease, hypertension Renal dysfunction - chronic renal failure,acute kidney disease. Pre-existing neurological deficits,psychiatric illness will be excluded from the study. If the laparoscopic surgery will be switched to open procedure, the patient will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Onset & duration of Sensory blockade Duration of post operative analgesia Visual analogue scoreTimepoint: 18 months

Secondary

MeasureTime frame
Postoperative rescue analgesic requirement Side effects or complicationsTimepoint: 18 months

Countries

India

Contacts

Public ContactDr Varun Sharma

Career institute of medical science and hospital

Dr.priyeshlpsc@gmail.com7985975077

Outcome results

None listed

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