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Ketorolac and Morphine for Renal Colic

Efficacy and Safety of Combination Therapy with Ketorolac and Morphine in Patient with Acute Renal Colic; A Triple-Blind Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201706032445N6
Enrollment
300
Registered
2017-06-07
Start date
2014-03-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Acute Renal Colic. Unspecified renal colic

Interventions

Intervention 1: 30mg Intravenous Ketorolac + 0.1 mg/kg Intravenous Morphine Sulphate. Intervention 2: 0.1 mg/kg Intravenous Morphine Sulphate. Intervention 3: 30mg Intravenous Ketorolac.
Treatment - Drugs
30mg Intravenous Ketorolac + 0.1 mg/kg Intravenous Morphine Sulphate
0.1 mg/kg Intravenous Morphine Sulphate
30mg Intravenous Ketorolac

Sponsors

Vice chancellor for research of Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age 18-55 years; Clinical diagnosis of acute renal colic (sudden sharp colic flank pain with or without radiation to genitalia or groin and with or without urinary symptoms); Pain score of 5 or more measured by 10-cm visual analogue scale (VAS). Exclusion criteria: history of kidney or renal dysfunction and severe dehydration; pregnancy; breastfeeding; single kidney or kidney transplantation; history of peptic ulcers and gastrointestinal bleeding; receiving analgesics within 6 hours before presentation; history of bleeding diathesis; history of cardiovascular disease and the use of angiotensin-converting-enzyme inhibitor (ACE inhibitor) or angiotensin receptor blockers (ARB); anticoagulant medication or coagulation disorders; history of drug dependence or current use of methadone or chronic consumption of tobacco and alcohol; peritonitis; presence of any peritoneal sign.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 0, 20 and 40 minutes. Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Adverse effects. Timepoint: 0, 20 and 40 minutes. Method of measurement: Clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehran Amooei Khanabbasi

Mazandaran University of Medical Sciences

farzadbozorgi1356@gmail.com+98 921 670 7983

Outcome results

None listed

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