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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

Evaluation of safety of hydrogel wound dressing based on polyacrylic acid and xanthan gums in patients with 2nd thickness burns (Clinical trial phase I)

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20161001030072N3
Enrollment
6
Registered
2023-05-10
Start date
2023-05-21
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Second degree burn. Burn and corrosion of head, face, and neck

Interventions

In the intervention group: before studying the wound, patients are examined by a doctor based on a checklist. Wounds are first washed with normal saline, Then a hydrogel dressing based on polyacrylic

Sponsors

Rasht University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Thermal burns with flame or boiling water Second degree burns Burn percent range less than 10% 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

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

Design outcomes

Primary

MeasureTime frame
Local out comes. Timepoint: At the beginning of the study (before the intervention) and 1, 3 and 7 days after applying the hydrogel wound dressing. Method of measurement: Clinical observations and filling the checklist in 4 time points.

Secondary

MeasureTime frame
Systemic outcomes. Timepoint: At the beginning of the study (before the intervention) and 1, 3 and 7 days after applying the hydrogel wound dressing. Method of measurement: Clinical observations and filling the checklist in 4 time points.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Mobayen

Rasht University of Medical Sciences

Maziar.mobayen@gmail.com+98 13 3336 8540

Outcome results

None listed

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