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Comparison between the clinical efficacy of Intravenous Fentanyl and Ketorolac in relieving renal colic pain

Comparison between the clinical efficacy of Intravenous Fentanyl and Ketorolac in relieving renal colic pain

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150902023855N3
Enrollment
110
Registered
2020-07-14
Start date
2020-06-03
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Acute Renal Colic. N20.2

Interventions

Intervention 1: Intervention group 1: patients will receive 0.1mg intravenous Fentanyl (Darou Pakhsh Pharmaceutical company) infused in 100 ml normal saline within 10 minutes. Intervention 2: Interven

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Patients with a history of unilateral abdominal or flank pain that the treating emergency physicians suspect to be renal colic Ultrasonography or CT Scan or intravenous pyelography (IVP) findings consistent with the diagnosis of renal stone Stone excretion

Exclusion criteria

Exclusion criteria: Visual Analog Scale (VAS)=3 History of peptic ulcer disease History of asthma History of bleeding disorder Using of oral anticoagulant Impaired renal or hepatic function Hypersensitivity to Aspirin or NSAID or Fentanyl Pregnant and breast-feeding women Received Sedative,Antipsychotic,MAO-I, painkillers within 6 hours before Younger than 18 and greater than 55 years old

Design outcomes

Primary

MeasureTime frame
Pain level. Timepoint: Before treatment initiation and sequentially at 20, 40, 60 minutes. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Heart rate. Timepoint: Before treatment initiation and sequentially at 20, 40, 60 minutes. Method of measurement: Radial puls.;Blood pressure. Timepoint: Before treatment initiation and sequentially at 20, 40, 60 minutes. Method of measurement: Sphygmomanometer.;Body temperature. Timepoint: Before treatment initiation and sequentially at 20, 40, 60 minutes. Method of measurement: Thermometer(axillary).;Respiratory rate. Timepoint: Before treatment initiation and sequentially at 20, 40, 60 minutes. Method of measurement: Physical exam.;Fentanyl side effects. Timepoint: In all the time in care. Method of measurement: Questionnaire and physical examination.;Ketorolac side effect. Timepoint: In all the time in care. Method of measurement: Questionnaire and physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Davood Arab

Semnan University of Medical Sciences

drdavoodarab@semums.ac.ir+98 23 3343 7830

Outcome results

None listed

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