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Diazepam and Methocarbamol in spinal trauma efficacy

The comparative study of clinical efficacy and palliative effect of adding Diazepam and Methocarbamol to Morphine in emergency department patients with spinal trauma

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130108012072N12
Enrollment
105
Registered
2020-11-27
Start date
2020-12-21
Completion date
Unknown
Last updated
2020-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal trauma. Other and unspecified injury of lumbar and sacral spinal cord

Interventions

Intervention 1: Intervention group 1: 0.1 mg/kg Morphine (osvahpharma) diluted in 100 ml normal saline in 10 minutes infusion. Intervention 2: Intervention group 2: 0.1 mg/kg Morphine (osvahpharma) an

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

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

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrdad Esmailian

Esfahan University of Medical Sciences

m_esmailian@med.mui.ac.ir+98 31 3629 3482

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026