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Analgesic effect of intravenous ketamine in patients with renal colic

Comparison of analgesic effect of intravenous low dose Ketamine and intravenous ketorolac ,in management of the acute pain in renal colic patients who admitted to the emergency department

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017021932660N1
Enrollment
126
Registered
2017-06-06
Start date
2016-03-19
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

Renal colic. Calculus of kidney and ureter

Interventions

Intervention 1: In Group A, patients receive a dose of 0.6mg / kg intravenous ketamine.Pain severity base on NRS and complication such as hypertention,Tachycardia ,nausea ,dizziness,agitation , will
Treatment - Drugs
In Group A, patients receive a dose of 0.6mg / kg intravenous ketamine.Pain severity base on NRS and complication such as hypertention,Tachycardia ,nausea ,dizziness,agitation , will be recorded at 5
In Group B, patients receive a dose of 30mg intravenous ketorolac.Pain severity base on NRS and complication such as hypertention,Tachycardia ,nausea ,dizziness,agitation , will be recorded at 5th, 1

Sponsors

Tehran University of Medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: all patient with high clinical suspicious of renal colic; all patient who come with pain and have clinical or lab data of renal colic. Exclusion criteria: age < 18 years; unwilling to study participation; past history of allergy to ketorolac or ketamine; Pregnancy or probable pregnancy; Breast feeding; history of analgesic drug consumption < 4 hours ago; liver; renal or heart failure patients; decrease level of consciousness; mental disability;fibromyalgia; Vascular lesions and brain lesions; History of opium addiction; Psychosis; Refusal of the patients from the participation;Head and eyes trauma

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The pain of kidney stones. Timepoint: 0 , 5 , 15 , 30 , 60 , 120 min. Method of measurement: Numeric Rating Scale.

Secondary

MeasureTime frame
Hypertention. Timepoint: 5, 15,30,60,120 min after intervention. Method of measurement: Using a questionnaire , Measurement of vital signs.;Tachycardia. Timepoint: 5, 15,30,60,120 min after intervention. Method of measurement: Using a questionnaire, measurement of vital signs.;Nausea. Timepoint: 5, 15,30,60,120 min after intervention. Method of measurement: Using a questionnaire.;Dizziness. Timepoint: 5, 15,30,60,120 min after intervention. Method of measurement: Using a questionnaire.;Agitation. Timepoint: 5, 15,30,60,120 min after intervention. Method of measurement: Using a questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mozhgan Farmahini Farahani

Tehran University of Medical sciences

farahanimozhgan@yahoo.com+98 21 7784 4341

Outcome results

None listed

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