MedPath

Efficacy of Ketamine on Acute Pai

Phase 3
Recruiting
Conditions
Acute pain.
Acute pain, not elsewhere classified
G89.1
Registration Number
IRCT20200608047684N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

Any adult patient (age>18) with acute pain who need analgesia

Exclusion Criteria

Pain score =5
Pregnancy and post-partum women
Altered mental status
Allergy to ketamine or fentanyl
Body weight = 46 kg or = 115
Unstable vital signs: BP= 90 mmHg or = 180 mmHg , PR=150 or =50 bits/min , RR=10 or =30
History of recent head or eye trauma
History of Siesure
History of elevated ICP
Chronic pain
Renal or hepatic failure
Substance or alcohol abuse
Documented psychiatric disorders
Opium addiction
Recent use of narcotic analgesics

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score by Verbal Numerical Rating Scale (VNRS). Timepoint: 5,10,15 and 30 minutes after administration of medications. Method of measurement: Verbal Numerical Rating Scale (VNRS).;Blood pressure. Timepoint: 5,10,15 and 30 minutes after administration of medications. Method of measurement: Sphygmomanometer.
Secondary Outcome Measures
NameTimeMethod
Agitation scale calculating with Richmond Agitation-Sedation Scale. Timepoint: When agitation appears. Method of measurement: Richmond Agitation-Sedation Scale.;Need for rescue analgesic. Timepoint: 10 minutes after administration of medications. Method of measurement: Asking from patient about presence of pain.
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