The Application of Infrared Thermography in the Prediction of Skin Healing in Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversitaire Ziekenhuizen KU Leuven

About this trial

This study investigates whether infrared thermography, a harmless and non-invasive thermal camera technique, can help monitor how surgical wounds heal after skin surgery. The goal is to detect wound problems earlier, such as infection or delayed healing, and to support doctors in making timely clinical decisions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures

Adult subjects (>18 years of age) at time of enrolment

Patients undergoing a surgical excision under local anesthesia

Indications of the excisions were skin lesions suspected to be malignant, skin lesions confirmed to be malignant via prior biopsy

Disqualifiers

Patient has history of pre-existing diabetes type I and II

Patients with pre-existing chronic wound problems

Patients with renal dysfunction,

Patients with venous insufficiency confirmed via radiographic imaging

Trial design

Design model

Single group

Treatments tested in this trial

  • Infrared thermography

    Device

    Participants will undergo non-contact infrared thermography using a handheld thermal imaging device to capture temperature patterns of the surgical wound at predefined postoperative time points. The device is used solely for diagnostic imaging and does not touch the skin or alter wound care. Thermal images are recorded under standardized conditions and analyzed to identify temperature changes that may indicate normal healing or early signs of complications such as infection, delayed healing, or graft failure. This intervention differs from standard clinical follow-up because it adds objective thermal measurements that are not part of routine postoperative assessment.

Treatment groups

120 Participants
are divided into 1 treatment group
Group A: Thermography Monitoring ArmExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Thermal pattern changes associated with normal versus abnormal surgical wound healing

Changes in wound temperature patterns detected through infrared thermography will be evaluated to determine whether they correspond to normal healing or early signs of complications such as infection, delayed healing, or graft problems. Thermal images will be analyzed for differences in temperature distribution, symmetry, and progression over time.

Time frame
Postoperative days 2-4 and day 7 for Mohs surgery; day 7 and day 14 for trunk and extremities; postoperative weeks 1-4 for scalp grafts.

Secondary outcomes

1

Overall feasibility and clinical utility of infrared thermography

This outcome assesses the overall feasibility and clinical utility of infrared thermography in postoperative wound monitoring, based on a combined evaluation of image acquisition success, clinician-reported usability, and its contribution to earlier identification of wound abnormalities. A single composite qualitative outcome will be reported.

Time frame
Postoperative days 2-4 and day 7 (Mohs); day 7 and day 14 (trunk/extremities); postoperative weeks 1-4 (scalp).

Other outcomes

Sponsors and contacts

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