Comparison of the effect of fentanyl with fentanyl and midazolam in pain control

Phase 3

Recruiting

• Conditions: Trauma.; Acute pain due to trauma; G89.11

• Registration Number: IRCT20201226049832N1
• Lead Sponsor: Shahroud University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 May 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 78

Inclusion Criteria

People in the age group of 18 to 80 year
Mechanism of trauma multiple trauma and direct trauma
Obtaining informed consent
Stable hemodynamic status (including patients with systolic blood pressure above 90 mm Hg)
Patient consciousness is complete (GCS = 15)

Exclusion Criteria

Pregnancy.Mentally retarded patients
Mentally retarded patients
Consumption of psychotropic drugs
Drug addicted patients

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain control in patient trauma. Timepoint: at the time of referral , 30 and 60 minutes after the intervention. Method of measurement: using the Visual Analogue Scale.

Secondary Outcome Measures

Name	Time	Method
Side effects of medications. Timepoint: 30 and 60 minutes after the intervention. Method of measurement: Examination by a specialist.;Level of anxiety. Timepoint: At the time of referral, 60 minutes after referral. Method of measurement: Depression Anxiety Stress Scale.