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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220113053709N1
Enrollment
40
Registered
2022-01-24
Start date
2021-12-22
Completion date
Unknown
Last updated
2022-02-07

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

Conditions

Renal colic. Unspecified renal colic

Interventions

Intervention 1: Intervention group: n the first group, which includes the spina erector block, using the 7.5 MHz (surface) probe of the ultrasound device, which is placed in the paravertebral region (

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Pain score. Timepoint: pain score in the start, 30 minute and 60 minute. Method of measurement: Iowa questionnaire.

Secondary

MeasureTime frame
Complication. Timepoint: start, 30 minute, 60 minute. Method of measurement: Checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Javad Darijani

Kerman University of Medical Sciences

j.darijani@kmu.ac.ir+98 34 3223 5011

Outcome results

None listed

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