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comparison of Nerve block and local infiltration method for pain relief after kidney stone surgery

To compare the efficacy of intercostal nerve block and peritubal block on postoperative pain management following percutaneous nephrolithotomy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/06/008821
Enrollment
60
Registered
2017-06-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- patients with renal stones

Interventions

Intervention1: intercostal nerve block at 10,11 and 12th intercostal spaces: intercostal nerve block at 10,11 and 12th intercostal spaces with 5ml of 0.5% ropivacaine under fluroscopic guidance. singl

Sponsors

Nizams institute of medical sciences for material and infrastructural support
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The patients enrolled were aged between 18 to 60 yrs, weighing 40 to 80kg and belonging to either gender scheduled for elective standard PCNL requiring 14/16 French nephrostomy tube at the end of procedure with single subcostal nephrostomy tract under general anesthesia. The average stone size was 2.5cm

Exclusion criteria

Exclusion criteria: Patients with renal stones requiring more than a single puncture with supracostal punctures, BMI >30, patients with uncontrolled diabetes& hypertension, excessive bleeding during the procedure, surgical procedure lasting more than 3 hrs duration patients with ASA grades III and IV, delayed recovery or requiring post-operative ventilation were excluded from the study.

Design outcomes

Primary

MeasureTime frame
The primary aim of the study present study was to investigate the efficacy of ICNB over peritubal infiltration with 0.5% ropivacaine under fluoroscopic guidance to alleviate postoperative pain after PCNL in terms of duration of analgesiaTimepoint: every 4 hours for 24 hrs

Secondary

MeasureTime frame
The secondary end point being number of analgesic demands, patient satisfaction and any complications thereby.Timepoint: every 4 hours for 24 hrs

Countries

India

Contacts

Public ContactDr Nirmala Jonnavithula

Nizams Institute of Medical Sciences Panjagutta

chirraspulse@yahoo.co.in9866006510

Outcome results

None listed

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