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Comparison of Nitrous Oxided and Ketamin Sedative Analgesic Effect for Pain Control.

Phase 2
Conditions
ocal anesthesia.
Local anaesthetics
Registration Number
IRCT2013111815446N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Inclusion Criteria: any limbs fractures who are seeking for Pain Control.

Exclusion Criteria

COPD; liver disease; head injury; loss of consciousness; lung injury; asthma and patient disagreement.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain relief. Timepoint: Baseline, fifth, tenth, fifteenth minutes. Method of measurement: VAS score.
Secondary Outcome Measures
NameTimeMethod
Decrease blood pressure. Timepoint: Baseline, fifth, tenth, fifteenth minutes since start of drug give. Method of measurement: Patient monitoring- blood pressure measurement.;Respiratory faillue. Timepoint: Baseline, fifth, tenth, fifteenth minutes since start of drug give. Method of measurement: Patient monitoring- blood pressure measurement.;Vomiting. Timepoint: Baseline, fifth, tenth, fifteenth minutes since start of drug give. Method of measurement: Patient monitoring- blood pressure measurement.
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