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NCT06716892Recruiting

Non-invasive Preoperative Tissue Evaluation in Head and Neck Tumor Patients Using Multispectral Optoacoustic Tomography (MSOT)

Non-invasive Preoperative Donor-site Evaluation of Free Flaps in Head and Neck Tumor Patients Using Multispectral Optoacoustic Tomography (MSOT)

Source: ClinicalTrials.gov · Last updated 4 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Multispectral Optoacoustic Tomography (MSOT) is a promising imaging technology that utilizes pulsed laser light. One of the key capabilities of this technology is measuring oxygenation within human tissue. This proposed study aims to investigate possible limitations of human tissue used for reconstructive surgery due to flawed tissue perfusion. Healthy volunteers as well as patients with a diagnosed head and neck cancer entity will be recruited. Both cohorts will then be scanned on different body areas (most common tissue sites used for reconstructive surgery on the back, arms and legs) to assess differences in muscle oxygenation between the healthy and tumor patient cohort using MSOT. The hypothesis of the study is, that patients with diagnosed head and neck cancer entities are prone to compromised tissue perfusion due to a high prevalence of smoking within the head neck tumor patient cohort and therefore perfusion restirciting diseases e.g. peripheral arterial occlusive disease (PAOD).

Status (registry)
Recruiting
Study type
Observational
Enrollment
40 (estimated)
First submitted
29 Nov 2024
Start date
28 Nov 2024
Primary completion date
30 Jun 2025
Lead sponsor
University of Erlangen-Nürnberg Medical School
NCT number
NCT06716892

What you commit to

  • Study type: Observational
  • Planned participants: 40
  • From 28 Nov 2024 to the primary completion date, 30 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Pregnancy / breastfeeding
  • ink / tattoo in the areas of interest (upper back, distal forearm, upper and lower leg)
  • missing consent form
  • Cohort 2: Chronical abuse of alcohol and nicotine.

Who the study is looking for

  • Cohort 1: Histopathological diagnosed head and neck tumor patients.
  • Cohort 2: Healthy adults.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Erlangen
Coordinator of this site? Confirm its status
ErlangenGermanyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.