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IN ADULT PATIENTS UNDERGOING PERCUTANEOUS NEPHROLITHOTOMY, INTERCOSTAL NERVE BLOCK(INTERVENTION) WITH ROPIVACAINE VERSUS ROPIVACAINE AND DEXAMETHASONE IS COMPARED FOR POST-OPERATIVE PAIN RELIEF

Comparison of Intercostal Nerve Block with ROPIVACAINE versus ROPIVACINE and DEXAMETHASONE for post-operative analgesia in adult patients undergoing PERCUTANEOUS NEPHROLITHOTOMY - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078775
Enrollment
80
Registered
2024-12-30
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: O- Medical and Surgical

Interventions

Intervention1: Ropivacaine 0.2% and dexamethasone 0.2mg/kg(10ml total volume): Intercostal Nerve Block in Intercostal space between 9th-10th rib/10th-11th rib/11th-12th rib in patients undergoing PERC

Sponsors

Jeet Thakkar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to consent for the study Age :18 to 75 years Either gender BMI-18-30 kg/m2 American Society of Anesthesiologist (ASA) Classification I, II, III Elective PCNL Surgery.

Exclusion criteria

Exclusion criteria: Patients with pre-existing uncontrolled respiratory and cardiac diseases, uncontrolled DM(ASA Grade 4 and 5) Obese patients, pregnant patients Patients with history of bleeding disorders or on anticoagulant therapy Patient refusal to participate in study. Infection at or near injection site Surgery procedure lasting more than 3 hours Renal stone requiring more than 1 puncture Delayed recovery or requirement of post operative ventilator support.

Design outcomes

Primary

MeasureTime frame
Time to first post-operative rescue analgesic Timepoint: 24 Hours

Secondary

MeasureTime frame
1.Post-operative requirement of Opioid Analgesic [Time-for 24 hours][Tramadol 1-2mg/kg IV] 2. Pain scoring by Numerical Rating Scale at 30 minutes,1,2,4,6,12,24 hours.[post-operatively] 3. Patient satisfaction scoring. 4.Incidence of Post Operative nausea and vomiting, respiratory or cardiac complications.Timepoint: 30 minutes,1,2,4,6,12,24 hours.

Countries

India

Contacts

Public ContactJeet Thakkar

B.J.MEDICAL COLLEGE,AHMEDABAD

seng_90@yahoo.com9825504948

Outcome results

None listed

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