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Bacterial nanocellulose wound dressings for the healing of second degree burn wounds

Comparison of bacterial nanocellulose wound dressings and standard treatment in the healing of second degree burn wounds: a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160117026069N6
Enrollment
24
Registered
2023-01-26
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Second degree burn ulcer. Calcification and ossification of muscles associated with burns

Interventions

Intervention 1: Intervention group: After preliminary and necessary measures such as washing and disinfecting the wound, nanocellulose coating is placed on the wound and covered with a sterile gauze.

Sponsors

Karaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Having second degree burns on the limbs or trunk (with TBSA below 10%)

Exclusion criteria

Exclusion criteria: Pregnancy Chronic heart, kidney and liver diseases Wound infection Systematic cortisone use

Design outcomes

Primary

MeasureTime frame
Duration of hospitalization. Timepoint: When the patient discharged from the hospital. Method of measurement: Information recorded in the patient file.;Duration of recovery. Timepoint: Daily until hospitalization and weekly visits thereafter. Method of measurement: Observation of the physician.

Secondary

MeasureTime frame
Itching. Timepoint: First day, second day, third day. Method of measurement: Asking the patient based on the VAS scale.;Wound infection. Timepoint: Daily during hospitalization and weekly visits thereafter. Method of measurement: Observation of the physician.;Hypertrophic scar. Timepoint: The last visit. Method of measurement: Observation of the physician.;Patient satisfaction. Timepoint: The last visit. Method of measurement: Questioning the patient in the form of yes or no.;Pain. Timepoint: First day, second day, third day. Method of measurement: Asking the patient based on the VAS scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHadi Pourjafar

Karaj University of Medical Sciences

pourjafarhadi59@gmail.com+98 26 3464 3705

Outcome results

None listed

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