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Comparison of ultrasound guided erector spinal plane block with intra-venous fentanyl in the management of refractory renal colic pai

Phase 3
Conditions
Renal colic.
Unspecified renal colic
Registration Number
IRCT20220113053709N1
Lead Sponsor
Kerman University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

The study population was patients 20-65 years who had renal colic.

Exclusion Criteria

Patients who had distracting injury
Patients who had not full consciousness or cognitive activity
Patients who had a history of allergies to Lidocaine and fentanyl
Patients who had diseases that interfere with the procedure or pain rating (such as bleeding defects or peripheral neuropathy)
Patients who did not agree to participate in the study or local block

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score. Timepoint: pain score in the start, 30 minute and 60 minute. Method of measurement: Iowa questionnaire.
Secondary Outcome Measures
NameTimeMethod
Complication. Timepoint: start, 30 minute, 60 minute. Method of measurement: Checklist.
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