Effectiveness of human amniotic membrane dressing on wound healing in plastic surgery patients

Evaluation of the effectiveness of human amniotic membrane dressing compared to conventional dressing on wound healing in plastic surgery patients

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20201113049373N5

Enrollment

Registered

2024-10-28

Start date

2024-10-22

Completion date

Unknown

Last updated

2025-01-08

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

Conditions

surgical incision stie scar. Hypertrophic scar

Interventions

Intervention 1: Intervention group: The surgical hemi incision, which is identified using randomization, and at the end of the surgery is covered by the amniotic membrane dressing , and the conventio

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients candidated for abdominoplasty and mammoplasty surgery

Exclusion criteria

Exclusion criteria: Patients with wound healing disorders

Design outcomes

Primary

Measure	Time frame
Scar assessment of the surgical incision site. Timepoint: 1 week and 1 and 6 months after surgery. Method of measurement: Scar evaluation using patient and observer scar assessment scale(posas), Vancouver scar scale(vss), Stony Brook scar evaluation scale(sbses).;Assessment of pain at the site of surgical incision. Timepoint: 1 week and 1 and 6 months after surgery. Method of measurement: with the patient and observer scar assessment scale tool.;Evaluation of pruritus at the site of surgical incision. Timepoint: 1 week and 1 and 6 months after surgery. Method of measurement: with the patient and observer scar assessment scale tool.	—

Measure

Time frame

Scar assessment of the surgical incision site. Timepoint: 1 week and 1 and 6 months after surgery. Method of measurement: Scar evaluation using patient and observer scar assessment scale(posas), Vancouver scar scale(vss), Stony Brook scar evaluation scale(sbses).;Assessment of pain at the site of surgical incision. Timepoint: 1 week and 1 and 6 months after surgery. Method of measurement: with the patient and observer scar assessment scale tool.;Evaluation of pruritus at the site of surgical incision. Timepoint: 1 week and 1 and 6 months after surgery. Method of measurement: with the patient and observer scar assessment scale tool.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactEhsan Rahimpour

Tehran University of Medical Sciences

dr.rahimpour83@gmail.com+98 21 2261 4448

Outcome results

None listed

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