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Investigating the effect of topical tranexamic acid on wound healing after excision of facial basal cell carcinomas

Investigating the effect of topical application of tranexamic acid on wound healing complications in patients undergoing reconstructive plastic surgery after excision of facial basal cell carcinomas : A randomized clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260412069054N1
Enrollment
46
Registered
2026-04-15
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Malignant neoplasm of connective and soft tissue of head, face, and neck. http://apps.who.int/classifications/icd10/browse/2010/en

Interventions

Intervention 1: Intervention group: After excision of the malignant lesion and before flap placement, the surgical site will be irrigated with a 3% TXA solution, and a TXA-soaked gauze will be applied

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age = 18 years Patients with basal cell carcinoma in the head region, including the face and scalp Reconstructive surgery using flap technique

Exclusion criteria

Exclusion criteria: Patients with a BMI = 35 Patients who are smokers Pregnant patients Patients with an American Society of Anesthesiologists (ASA) score greater than 3 Patients taking anticoagulant or antiplatelet medications Patients with uncontrolled comorbidities Patients with a history of receiving neoadjuvant therapy Patients with a history of prior surgery in the head region Patients with a previous history of thromboembolic events, autoimmune diseases, or hematologic disorders

Design outcomes

Primary

MeasureTime frame
Postoperative ecchymosis. Timepoint: Patients will be evaluated for outcomes at 24 hours postoperatively, as well as at 7 days, 28 days, and 3 months after surgery. Method of measurement: Examination of the surgical site and assessment of the occurrence ecchymosis (or not).

Secondary

MeasureTime frame
Intraoperative blood loss; other postoperative complications (hematoma, flap ischemia/necrosis, surgical site infection, thromboembolic events, hypertrophic scar, keloid); the need for reoperation; length of hospital stay (days); and hospital readmission will be assessed. The surgical scar status will be evaluated at the end of the 3-month follow-up. Timepoint: Patients will be evaluated for outcomes at 24 hours postoperatively, as well as at 7 days, 28 days, and 3 months after surgery. Method of measurement: The Boezzart scale will be used to assess the intraoperative bleeding. Postoperative complications will be evaluated through patient examination and inspection of the surgical site to determine the presence or absence of any events. At the end of the 3-month follow-up, the following questionnaire will be used to assess the surgical scar condition: the Patient and Observer Scar Assessment Scale (POSAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Sharifi

Mashhad University of Medical Sciences

SharifiRZ@mums.ac.ir+98 51 3801 2000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026