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Effect of topical ketamine on pain relief

Phase 3
Conditions
...
Registration Number
IRCT20180129038549N2
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
75
Inclusion Criteria

All adult patients referred to the emergency department of al-Zahra and Kashani hospitals
Need for Peripheral Intravenous Cannulation
Alert

Exclusion Criteria

The presence of visual, mental and verbal disorders
Opioids addiction
Sensitivity to anesthetic drugs
Patients in a life-threatening condition
Analgesic drug addict(More than 4 times a week)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The severity of pain. Timepoint: After intravenous cannulation. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
Time to start anesthetic effect. Timepoint: To an hour of exposure. Method of measurement: Time (minute).;Drug side effects such as redness, whitening and skin blemishes. Timepoint: Until the time of discharge. Method of measurement: Observation.
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