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Effect of fibrin glue enriched with platelets and stapler in burn patients

Investigating the Effect of Fibrin Glue Enriched with Platelets Compared to Stapler on the Faster Clinching of Skin Autografts Lesions in Burn Patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130819014404N3
Enrollment
56
Registered
2019-04-28
Start date
2019-05-22
Completion date
Unknown
Last updated
2019-05-21

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

Conditions

Condition 1: Burns of head, face, and neck. Condition 2: Burns of trunk. Condition 3: Burns of shoulder and upper limb. Condition 4: Burns of wrist and hand. Condition 5: Burns of lower limb. Condition 6: Burns of ankle and foot. Condition 7: Burns of multiple body regions. Burn and corrosion of head, face, and neck Burn and corrosion of trunk Burn and corrosion of shoulder and upper limb, except wrist and hand Burn and corrosion of wrist and hand Burn and corrosion of lower limb, except an

Interventions

Intervention 1: Intervention group: Surgical biological adhesive
Fibrin glue which is produced by the Microwave Company of France and the Tisceon brand. Intervention 2: Control group: Stapler.

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who had burn injuries. Burn lesions that need graft.

Exclusion criteria

Exclusion criteria: Diabetes. Collagen vascular disease or hemorrhagic disorders. Consuming anticoagulants or steroids drugs. Being allergic to local anesthesia or Bacitracin. Patient dissatisfaction.

Design outcomes

Primary

MeasureTime frame
The improvement of patients' skin. Timepoint: One, three and four weeks after surgery. Method of measurement: Clinical evaluation.

Secondary

MeasureTime frame
Condition of skin infection. Timepoint: One, three and four weeks after surgery. Method of measurement: Clinical evaluation and wound culture.;The condition of skin graft. Timepoint: At 8th week after surgery (followup). Method of measurement: Clinical evaluation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Hasan Tavousi

Mashhad University of Medical Sciences

TavoosiH@mums.ac.ir+98 51 3854 3031

Outcome results

None listed

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