Assessing the result of dermal graft without suture fixation in burn patients

Assessing the result of dermal graft without suture fixation in burn patients: a clinical trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT201610029014N118

Enrollment

Registered

2016-10-03

Start date

2016-04-08

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Condition 1: Burn. Condition 2: Burn. Condition 3: Burn. Burn and corrosion of head and neck Burn and corrosion of trunk Burn and corrosion of shoulder and upper limb, except wrist and hand

Interventions

Dermal graft without suture fixation.

Treatment - Surgery

Dermal graft without suture fixation

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria: burn patients who are candidate for dermal graft. Exclusion criteria: Sensitivity to anesthesia medications; contraindication of general or spinal anesthesia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Assessing the result of dermal graft without suture fixation. Timepoint: 5 days after surgery. Method of measurement: through physical examination.	—

Secondary

Measure	Time frame
Assessing local hematoma or bleeding at surgical location. Timepoint: 5 days after surgery. Method of measurement: through physical examination.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Abbas Ali Eskandarion

Besat Hospital

pjsk625@yahoo.com+98 81 3364 0030

Outcome results

None listed

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