The effective of opioid-ketamine on pain relief in traumatic patients

Phase 2

Recruiting

• Conditions: Condition 1: Traumatic arthropathy. Condition 2: injuries of head. Condition 3: Injury of abdominal. Condition 4: Injury of hand region. Condition 5: Injury of hand leg.; Traumatic arthropathy; Other and unspecified injuries of head; Injury of abdominal aorta; Combined traumatic amputation of (part of) finger(s) with other parts of wrist and hand; Traumatic amputation of one foot and other leg [any level, except foot]

• Registration Number: IRCT20181021041399N1
• Lead Sponsor: Artesh University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Aged between 15 and 40 years
Having a natural intelligence
No speech problem
according to the diagnosis patients with trauma require the analgesic

Exclusion Criteria

Allergy to the drugs studied
Having underlying disorder of respiratory, cardiac, neurological
Addicted
Active psychosis
Poisoning clinical

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain relief. Timepoint: before, 15 and 30 minutes. Method of measurement: visual analog scale.

Secondary Outcome Measures

Name	Time	Method
Side-effects of medications (nausea and vomiting, dizziness, dry mouth, euphoria, skin rash in the area of injection, nystagmus, tinnitus, etc). Timepoint: before, 15 and 30 minutes after intervention. Method of measurement: Designed questionnaire.