Evaluation of effect of pantoxyfylline in burned patients

Not Applicable

• Conditions: Condition 1: Burn. Condition 2: Burn. Condition 3: Burn. Condition 4: Burn. Condition 5: Burn. Condition 6: Burn.; Burn and corrosion of head and neck; Burn and corrosion of shoulder and upper limb, except wrist and hand; Burn and corrosion of trunk; Burn and corrosion of wrist and hand; Burn and corrosion of hip and lower limb, except ankle and foot; Burn and corrosion of ankle and foot

• Registration Number: IRCT2017050133737N1
• Lead Sponsor: Vice Chancellor for Research, Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

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

Inclusion Criteria

Inclusion criteria : Burn above 40% of body surface; Admission in maximum of an hour.
Exclusion criteria : Known comorbidities such as renal and heart faliure and respiratory disorders; Any other type of trauma; Disagree of patient or first degree relatives for participating in study.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Serum levels of IL-1and IL-6. Timepoint: At admission time and days 3,5 and 7. Method of measurement: Measuring serum levels.;Days of admission to ICU. Timepoint: From admission to discharge. Method of measurement: Registered by days and hours.;Death or discharge. Timepoint: From admission to discharge or death. Method of measurement: Registered outcome.