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To Study the Efficacy of ropivacaine 0.2percentage vs ropivacaine 0.2percentage with nalbuphine for post operative analgesia in appendicectomy patients by transversus abdominis plane block

To Study the Efficacy of Ropivacaine 0.2 percentage vs Ropivacaine 0.2 percentage with Nalbuphine for Post operative Analgesia in appendicectomy patients by Transversus Abdominis Plane Block - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083201
Enrollment
50
Registered
2025-03-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: K353- Acute appendicitis with localizedperitonitis

Interventions

Intervention1: Transversus abdominis plane block: the patient is placed in the supine position. After standard aseptic precautions, a blunt-tip 22-gauge, 80 100 mm short-bevel needle is inserted perpe

Sponsors

Parshant bansal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with American society of Anaesthiologist s physical status class 1&2 2.Patients posted for uncomplicated open Appendicectomy surgeries 3.Patients aged between 21-65 years of both genders who upon being explained the procedure are willing to participate in the study

Exclusion criteria

Exclusion criteria: 1. complicated appendectomies 2. Appendicular mass/abscess. 3. Skin infection at Puncture site. 4. Allergy to local anaesthetics. 5. Preoperative opioid and non-steroidal drug treatment for chronic pain treatment 6. Patients with blood dyscrasias, use of introoperative opiate analgesics, patients with significant hepatic, renal, cardiovascular, pulmonary, metabolic, psychiatric disorders

Design outcomes

Primary

MeasureTime frame
1.Post operative pain score(visual analog score-VAS) will be assessed 2. to study postoperative Analgesic duration, and analgesic pattern with 0.2%Ropivacaine 3. To study, post operative analgesic duration, and analgesic pattern with 0.2% Ropivacaine with Nalbuphine Timepoint: 30min,1 hr,4hr,8hr,12hr,16hr,20hr and 24hr.

Secondary

MeasureTime frame
1)To study, side-effects, if any. 2)To study additional post-operative analgesic requirementTimepoint: first 24 hours

Countries

India

Contacts

Public ContactDrSandipbhai Patel

Shri Bhausaheb Hire Government Medical college

sandip2027@yahoo.co.in9850878200

Outcome results

None listed

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