Diazepam and Methocarbamol in spinal trauma efficacy

Phase 3

• Conditions: Spinal trauma.; Other and unspecified injury of lumbar and sacral spinal cord; S34.1

• Registration Number: IRCT20130108012072N12
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 November 2020

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

Visual Analog Scale>4
No neurological signs
No malignancy and underling disease
No sensitivity to Morphine or Diazepam or Methocarbamol
Blood Pressure >=110/70 mm Hg

Exclusion Criteria

Drug user
History of Opiods, Non-steroidal anti-inflammatory drugs (NSAID's) and muscle relaxant drug use in past 24 hours

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain severity score with Visual Analog Scale. Timepoint: Study beginning, 30 minutes and 1 hour and 2 hours after treatment. Method of measurement: Visual Analog Scale.;Drug complications. Timepoint: Study beginning, 30 minutes and 1 hour and 2 hours after treatment. Method of measurement: Standard questionnaire form (Brief Medication Questionnaire).

Secondary Outcome Measures

Name	Time	Method
Insufficient pain control. Timepoint: 1 hour after treatment. Method of measurement: Visual Analog Scale.