Stimulation of cathodic, anodic, alternating current and EMLA anesthetic ointment on pain level and comfort in painful hospital procedures

Phase 3

Recruiting

• Conditions: Pain.; G89.1; Acute pain, not elsewhere classified

• Registration Number: IRCT20240123060780N1
• Lead Sponsor: Kermanshah University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

Full consciousness, literacy, reading, writing, verbal ability and healthy vision, no addiction, the skin of the study area should be healthy, no peripheral edema in the intervention area, not taking sedatives and anesthetic during the last 24 hours, not having a pacemaker and implantable cardiac device and defibrillators, no history of diabetes and vascular diseases.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Immediately and in minutes 1, 3 and 5. Method of measurement: The visual analog scale.

Secondary Outcome Measures

Name	Time	Method
Comfort level. Timepoint: 5 minutes after each procedure. Method of measurement: The visual analog scale.;Heart rate. Timepoint: Before, immediately and in 1,3,5 minutes. Method of measurement: Using portable pulse oximetry.