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Effect of ketamine and morphine in pain management of renal colic

Comparison of Low dose Ketamin plus Morphine versus Morphine alone in acute pain management of severe renal colic

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201109297667N1
Enrollment
100
Registered
2012-03-14
Start date
2012-02-26
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: One group received morphine 0.1 mg/kg intravenous and ketamine (0.1 mg/kg/dose intravenous , maximum dose = 0.4 mg/kg),. Intervention 2: another group received Morphine ( 0.1 mg/kg i
Treatment - Drugs
One group received morphine 0.1 mg/kg intravenous and ketamine (0.1 mg/kg/dose intravenous , maximum dose = 0.4 mg/kg),
another group received Morphine ( 0.1 mg/kg intravenous ) and placebo

Sponsors

Tehran University of Medical Sciences-Deputy for research affairs
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Previous nephrolithiasis , age between 18 to 50 years old, severity of pain at least 6 from 10, systolic blood pressure >= 90 mmHg, heart rate = 60-120/m, respiratory rate = 8-22/m, o2sat >= 90%, no addiction to opiate or psychiatric drugs, no use analgesic drugs or opioid before recording the data, no history of chronic liver disease or kidney or respiratory disease, no history of coagulopathy or blood disorders or chronic psychiatric disorder, no use of psychiatric drugs. Exclusion criteria: The patient who is not interested in study, addiction to opiate or psychiatric drugs, allergy to morphine or ketamine, inability to perception of VAS

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of pain. Timepoint: Before prescription the medication, 10, 30, 60, 90 and 120 minutes after medication. Method of measurement: VAS ( visual analog scale).

Secondary

MeasureTime frame
Nausea. Timepoint: Before prescription the medication, 10, 30, 60, 90 and 120 minutes after medication. Method of measurement: Questionnaire.;Agitation. Timepoint: Before prescription the medication, 10, 30, 60, 90 and 120 minutes after medication. Method of measurement: Questionnaire.;Diplopia. Timepoint: Before prescription the medication, 10, 30, 60, 90 and 120 minutes after medication. Method of measurement: Questionnaire.;Hallucination. Timepoint: Before prescription the medication, 10, 30, 60, 90 and 120 minutes after medication. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Bidi nader

Tehran University of Medical Sciences

n-bidi@razi.tums.ac.ir; bidi.nader@gmail.com+98 21 6652 5327

Outcome results

None listed

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