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Investigation of the effect of hydrogel wound dressing based on polyacrylic acid and xanthan gum in the treatment of burn injury

Phase 3
Recruiting
Conditions
Second degree burn.
Burn of unspecified degree of head, face, and neck
T20.0
Registration Number
IRCT20161001030072N4
Lead Sponsor
Rasht University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
42
Inclusion Criteria

Thermal burns with flame or boiling water
Second degree burns
Burn percent range Between 20-50%
Refer to the treatment center within less than 24 hours after the burn
Normal hemoglobin and total protein levels are normal
Male or female patients in age range 18 to 65 years
Written consent form by the patients
Body mass index between 18-30 kg/m2

Exclusion Criteria

Having background diseases ( anemia, diabetes, cardiovascular diseases, immunodeficiency disorder)
Lactating women Pregnant women

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ocal out comes. Timepoint: At the beginning of the study (before the intervention) and 1, 3, 7, 14 and 28 days after applying the hydrogel wound dressing. Method of measurement: Clinical observations and filling the checklist in 6 time points.;Systemic outcomes. Timepoint: At the beginning of the study (before the intervention) and 1, 3, 7, 14 and 28 days after applying the hydrogel wound dressing. Method of measurement: Clinical observations and filling the checklist in 6 time points.
Secondary Outcome Measures
NameTimeMethod
Infection. Timepoint: At the beginning of the study (before the intervention) and 1, 3, 7,14, and 28 days after applying the hydrogel wound dressing. Method of measurement: Based on examination done by evaluators.;Hospital stay. Timepoint: At discharge. Method of measurement: Based on patients' files.;Total fluid requirement. Timepoint: At discharge. Method of measurement: Based on patients' files.;Graft to TBSA (total body surface area) percent ratio. Timepoint: At the admission. Method of measurement: Measurements based on Wallace criteria.
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