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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04835116
Other study ID # AFIU Rawalpindi
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date April 11, 2019
Est. completion date October 11, 2019

Study information

Verified date April 2021
Source Armed Forces Institute of Urology, Rawalpindi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The rationale of this study was to compare the efficacy of peri-tract bupivacaine infiltration with intravenous post-operative analgesia following PCNL in reference to the context with the previous studies so that we can adopt the better technique to curtail the post-operative pain.


Description:

The rationale of this study was to compare the efficacy of peri-tract bupivacaine infiltration with intravenous postoperative analgesia following PCNL in reference to the context with the previous studies so that we can adopt the better technique to curtail the post-operative pain.


Recruitment information / eligibility

Status Completed
Enrollment 68
Est. completion date October 11, 2019
Est. primary completion date October 11, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 65 Years
Eligibility Inclusion Criteria: - all patients undergoing PCNL - age from 12-65 years - normal renal functions - no history of chronic pain - ASA I, II & III - Both genders Exclusion Criteria: - history of local anaesthesia allergy - Redo PCNL - Multiple punctures during PCNL - Excessive intra-operative bleeding - Diabetes mellitus - Coagulopathy - Mental disorder - ASA IV & V - Active urinary tract infection.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Bupivacaine Hydrochloride 0.25% Injection. Paracetamol 650mg. Orphenadrine 50mg.
Group A patients were administered per-operative peri tract local anesthesia infiltration with 0.25% bupivacaine augmented by post-operative oral analgesia with a combination of Paracetamol 650 mg and Orphenadrine 50mg 6 hourly.
paracetamol 1000mg. Tramadol 50mg. Dimenhydrinate 50mg.
Group B patients were only given post-operative intra-venous analgesia by Paracetamol 1gm intravenous 8 hourly augmented with a combination of Tramadol 50mg and Dimenhydrinate 50mg as and when required

Locations

Country Name City State
Pakistan Armed Forces Institute of Urology. Rawalpindi Punjab

Sponsors (1)

Lead Sponsor Collaborator
Armed Forces Institute of Urology, Rawalpindi

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of Post-Operative Analgesia With Peri Tract Local Anesthesia Infiltration and Oral Analgesia Versus Post-Operative Intravenous Analgesia After Percutaneous Nephrolithotomy. Efficacy of peri-tract infiltration of bupivacaine over standard oral analgesia in patients undergoing PCNL.
Measurement: Postoperative pain Measurement tool: Visual analog scale
6 months
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