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Completed

NCT Number: NCT04437030

Multiparametric Photoacoustic Imaging in the Course of Radiation Therapy of Malignant Head and Neck Tumors

Multispectral photoacoustic imaging enables the measurement of the optical absorption of various tissue components or exogenous contrast agents in vivo. The dominant, near infrared absorbing chromophores in human tissue are oxy- and deoxyhemoglobin followed by collagen, melanin and lipids. The multispectral measurement of the absorption of hemoglobin shows changes in blood oxygen saturation and blood volume. The high resolution of photoacoustic imaging also enables the vascular structure to be displayed. The aim of this exploratory study is to generate hypotheses by applying photoacoustic imaging to the field of head and neck tumor therapy. The next step is to investigate whether and how photoacoustic imaging can help improve diagnostics and better planning of treatments in the future. In particular, the differences between normal and tumor tissue and the changes in the tissue due to radiation therapy using photoacoustic imaging are examined. In the quantitative analysis of the images, measured chromophores, primarily oxygen saturation, blood volume and collagen concentrations at different measuring points are used in the course of the therapy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hopsital Heidelberg

Heidelberg, 69120, Germany

About this study

Multispectral photoacoustics enable non-invasive, inexpensive and dose-free real-time imaging of light-absorbing molecules (absorbers), e.g. Deoxyhemoglobin and oxygenated hemoglobin in human tissue. This allows blood oxygen saturation (sO2) to be determined at depths of up to several centimeters. Measurements of correlates to blood volume and collagen concentration are also made possible. In photoacoustic imaging, the tissue to be examined is irradiated with nanosecond short, near-infrared (650 - 1300nm) laser pulses. If laser light is locally absorbed by a tissue structure, it expands thermoelastically, which triggers an ultrasonic pressure wave, which is measured with the aid of an ultrasonic head. The initial pressure distribution and thus the absorption in the tissue can then be reconstructed. Since different molecules show distinct absorption behavior depending on the wavelength in the near infrared, by acquiring several wavelengths it is possible to estimate which absorbers are in which concentration in a tissue structure. The effectiveness and tolerability of modern high-precision radiation therapy for head and neck tumors largely depends on the quality of the imaging. The potential diagnostic benefits of photoacoustics in the radiotherapy of patients with head and neck tumors principally concern the target volume definition, the implementation of image-guided, adaptive radiotherapy and imaging tumor follow-up as well as the early detection of tumors.

Multispectral photoacoustics primarily enable the analysis of tumor hypoxia, which has been associated several times with increased radio resistance and an unfavorable prognosis. In addition, other factors, e.g. the blood volume and the collagen content in the tissue are analyzed.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Willingness and ability to participate
  • sufficient knowledge of German to understand the patient / subject information and the declaration of consent,
  • tumor disease to be treated by radiotherapy in the neck and neck area,
  • Completed wound healing after operative interventions in the head and neck area,
  • The patient's consent and written consent,
  • the patient's ability to assess the nature and scope as well as possible consequences of the clinical study,
  • Age ≥ 18 years.

Requirement 3 does not apply to the control group of healthy subjects

Exclusion criteria

  • Pre-radiation in the head and neck area
  • Inadequate regression of toxicities from previous therapies
  • Indications that the participant is unlikely to adhere to the study protocol (e.g. lack of compliance)
  • Missing written declaration of consent

Treatment and study plan

MSOT Acuity Echo device

Device

The MSOT acutiy Echo device can take ultrasound recordings in addition to photoacoustic recordings.

Primary outcomes

  1. diagnostic feasibility of photoacoustic imaging: Oxygen Saturation

    Time frame: previouse to Radiotherapy start

    Measurement of Oxygen Saturation in the tumor tissue

  2. diagnostic feasibility of photoacoustic imaging: Oxygen Saturation

    Time frame: 3 weeks after Radiotherapy start

    Measurement of Oxygen Saturation in the tumor tissue

  3. diagnostic feasibility of photoacoustic imaging: Oxygen Saturation

    Time frame: 3 month after Radiotherapy start

    Measurement of Oxygen Saturation in the tumor tissue

  4. diagnostic feasibility of photoacoustic imaging: blood volume

    Time frame: previouse to Radiotherapy start

    blood volume

  5. diagnostic feasibility of photoacoustic imaging: blood volume

    Time frame: 3 weeks after Radiotherapy start

    blood volume

  6. diagnostic feasibility of photoacoustic imaging: blood volume

    Time frame: 3 month after Radiotherapy start

    blood volume

  7. diagnostic feasibility of photoacoustic imaging: blood volume

    Time frame: previouse to Radiotherapy start

    amount of collagen in the tumor tissue

  8. diagnostic feasibility of photoacoustic imaging: amount of collagen in the tumor tissue

    Time frame: 3 weeks after Radiotherapy start

    amount of collagen in the tumor tissue

  9. diagnostic feasibility of photoacoustic imaging: amount of collagen in the tumor tissue

    Time frame: 3 month after Radiotherapy start

    amount of collagen in the tumor tissue

Secondary outcomes

  1. Analysis of Tumor tissue and normal tissue

    Time frame: previouse to Radiotherapy start

    Differences of Oxygen saturation

  2. Analysis of Tumor tissue and normal tissue

    Time frame: 3 weeks after Radiotherapy start

    Differences of Oxygen saturation

  3. Analysis of Tumor tissue and normal tissue

    Time frame: 3 month after Radiotherapy start

    Differences of Oxygen saturation

  4. Analysis of Tumor tissue and normal tissue

    Time frame: previouse to Radiotherapy start

    blood volume

  5. Analysis of Tumor tissue and normal tissue

    Time frame: 3 weeks after Radiotherapy start

    blood volume

  6. Analysis of Tumor tissue and normal tissue

    Time frame: 3 month after Radiotherapy start

    blood volume

  7. Analysis of Tumor tissue and normal tissue

    Time frame: previouse to Radiotherapy start

    amount of collagen

  8. Analysis of Tumor tissue and normal tissue

    Time frame: 3 weeks after Radiotherapy start

    amount of collagen

  9. Analysis of Tumor tissue and normal tissue

    Time frame: 3 month after Radiotherapy start

    amount of collagen

  10. multimodal information about tissue morphology

    Time frame: previouse to Radiotherapy start

    Registration of photoaccustic and MRI/CT Imaging

  11. multimodal information about tissue function

    Time frame: 3 weeks after Radiotherapy start

    Registration of photoaccustic and MRI/CT Imaging

  12. multimodal information about tissue function

    Time frame: 3 month after Radiotherapy start

    Registration of photoaccustic and MRI/CT Imaging

Sponsors and collaborators

Lead sponsor

University Hospital Heidelberg

Other

Registry information

Important dates

Study start
2020
Primary completion
2022
Study completion
2023
First posted
Jun 18, 2020
Registry last updated
Jan 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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