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Comparison of intravenous ibuprofen and intravenous ketorolac in renal colic pain reduction

Comparison of intravenous ibuprofen and intravenous ketorolac in renal colic pain reduction in the emergency department

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150213021063N5
Enrollment
195
Registered
2019-01-15
Start date
2018-10-23
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

Unspecified renal colic. Unspecified renal colic

Interventions

Intervention 1: The first intervention group (group I): 5 mg intravenous morphine sulfate in 5 minutes + 800 mg intravenous ibuprofen in 200 milliliters normal saline in 30 minutes + 2 milliliters int

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with renal colic who present to the emergency department and their pain intensities are equal or greater than 7 out of 10

Exclusion criteria

Exclusion criteria: History of an allergic reaction to ASA or other NSAIDs (including asthma, skin reactions, anaphylaxis, or ...) Known chronic kidney disease Age below 18 or above 65 years Weight below 50 kilograms Peptic ulcer disease history Gastrointestinal bleeding history Suspected volume deficit (based on mucous membranes) Any active bleeding Bleeding diathesis Using anticoagulant or antiplatelet drugs Known heart failure Pregnancy Lactation Systolic blood pressure lower than 100 mmHg

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before drug administration, 30, 60, and 120 minutes after drug administration. Method of measurement: Numeric rating scale.;Adverse events. Timepoint: Patients will be monitored continuously for adverse events since drug administration till patient discharge. Method of measurement: Specific occurred adverse event.;Patient's length of stay. Timepoint: At the time of patient discharge. Method of measurement: Minutes.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArash Safaie

Tehran University of Medical Sciences

a-safaie@sina.tums.ac.ir+98 216312413

Outcome results

None listed

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