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NIR Device for Assessment of Skin Flap Perfusion in Breast Surgery: A Pilot Interventional Study (ADisIRast)

29. Juni 2026 aktualisiert von: Valentina Hartwig, National Research Council, Institute of Clinical Physiology, Italy

ADisIRast: Applicazione Del Dispositivo NIR Nella Breast Unit. Studio Pilota Monocentrico, Non Randomizzato, Interventistico Con Dispositivo Medico, Premarket, Non Profit, Per la Valutazione Della Perfusione Del Lembo Cutaneo Pre e Post Operatoria

The goal of this single-center, nonrandomized, interventional non-profit pilot study is to evaluate the feasibility and clinical utility of a non-invasive near-infrared spectroscopy (NIRS) imaging device for assessing skin-flap tissue oxygen saturation in adult women undergoing mastectomy and immediate breast reconstruction after oncological surgery.

The main questions it aims to answer are:

  • Can NIRS imaging provide reproducible measurements of tissue oxygen saturation (StO₂) in mastectomy skin flaps before surgery, during the intraoperative phase, and during postoperative follow-up?
  • Can spatial and temporal variations in StO₂ identify areas of potentially reduced flap perfusion or impaired tissue viability?
  • Can NIRS-derived oxygenation measurements support the assessment of postoperative flap healing and ischemic complications?

Participants will:

  • undergo non-invasive NIRS imaging of the breast skin flap before surgery;
  • undergo one intraoperative NIRS acquisition during mastectomy and immediate breast reconstruction;
  • undergo repeated NIRS imaging during postoperative follow-up visits;
  • receive standard surgical treatment and postoperative care according to routine clinical practice.

NIRS imaging is performed for study purposes and does not influence intraoperative surgical decision-making or the choice of reconstructive procedure.

Studienübersicht

Status

Abgeschlossen

Intervention / Behandlung

Detaillierte Beschreibung

The ADISIRAST study is a single-center, non-randomized, pre-market, non-profit clinical investigation of a non-invasive near-infrared spectroscopy (NIRS) imaging device for the assessment of perfusion in mastectomy skin flaps in patients undergoing breast surgery with immediate reconstruction.

Mastectomy skin-flap viability is an important determinant of postoperative healing and reconstructive outcomes. In routine clinical practice, flap perfusion is mainly assessed through intraoperative inspection and surgical judgment. Objective methods for evaluating tissue oxygenation may provide complementary information and may help characterize regional perfusion patterns that are not readily apparent during standard clinical assessment.

Near-infrared spectroscopy is a non-invasive optical technique that estimates superficial tissue oxygen saturation (StO₂) by analyzing the relative absorption of near-infrared light by oxygenated and deoxygenated hemoglobin. The investigational device is a portable, non-contact NIRS imaging system that generates two-dimensional maps of superficial tissue oxygen saturation. The device does not require tissue contact, contrast-agent injection, or exposure to ionizing radiation. Acquisitions are performed by positioning the device at a standardized distance from the surgical area and obtaining a digital image together with the corresponding StO₂ map.

The study was designed to evaluate the feasibility, repeatability, and clinical interpretability of NIRS-derived StO₂ measurements in breast skin flaps throughout the perioperative period. NIRS images were acquired at predefined study time points, including a preoperative baseline assessment, an intraoperative assessment, and postoperative follow-up assessments(1 day and 15 days postoperative). This approach allowed the characterization of temporal changes in tissue oxygenation and the evaluation of regional differences within the skin flap.

Image analysis included assessment of absolute StO₂ values, regional oxygenation differences, spatial distribution of tissue areas within predefined StO₂ ranges, and longitudinal changes in oxygenation patterns. Regions of interest were defined within superior and inferior portions of the breast skin flap to explore regional perfusion heterogeneity. Additional image-derived metrics were calculated to quantify the extent of tissue area within selected StO₂ ranges and the degree of spatial heterogeneity of oxygenation.

Clinical and surgical data were prospectively collected, including reconstructive information, perioperative characteristics, postoperative flap healing, and clinically observed complications. NIRS findings were subsequently evaluated in relation to postoperative clinical observations, particularly the presence, location, and evolution of areas showing impaired healing or suspected ischemic changes.

Surgical planning and intraoperative decisions, including the choice of reconstructive approach, were made according to standard clinical practice, based on the treating surgical team's clinical assessment and preoperative evaluation. The operating surgeon was blinded to the intraoperative NIRS images, and NIRS findings did not influence surgical decision-making or the selection of the reconstructive procedure.

After study completion, NIRS-derived perfusion findings were retrospectively compared with the reconstructive strategy selected during surgery. This exploratory analysis was performed to assess the concordance between NIRS-based indications of flap perfusion and the clinical decision made by the surgical team. The analysis was intended to explore the potential future role of non-invasive tissue oxygenation imaging as an adjunctive tool for perioperative assessment and surgical training, rather than to evaluate a device-guided management strategy.

The study does not compare alternative surgical treatments or reconstructive techniques. It is designed as a feasibility and performance investigation and is not powered to establish definitive diagnostic thresholds, predict clinical outcomes with definitive accuracy, or demonstrate superiority of one reconstructive strategy over another. Data were collected prospectively and managed using coded participant identifiers.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

20

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

      • Pisa, Italien, 56126
        • U.O. Senologia, Azienda Ospedaliero-Universitaria Pisana (AOUP) Presidio Ospedaliero Santa Chiara

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  • Female sex, aged 18 to 90 years.
  • Breast cancer patients scheduled for mastectomy with immediate reconstruction using an implant or tissue expander; or healthy BRCA mutation carriers scheduled for prophylactic mastectomy.
  • No previous radiotherapy to the chest wall.
  • No previous neoadjuvant chemotherapy.

Exclusion Criteria:

  • Severe psychiatric disorders.
  • Advanced malignancy.
  • Severe aortic stenosis.
  • Obstructive hypertrophic cardiomyopathy.
  • Severe chronic kidney disease.
  • Severe chronic obstructive pulmonary disease.
  • Uncontrolled diabetes mellitus.
  • Advanced peripheral arterial occlusive disease (Leriche-Fontaine class III).
  • Use of benzodiazepines, non-benzodiazepine hypnotics, typical or atypical antipsychotics, antidepressants, or anticonvulsants without a stable dose for at least 4 months.
  • Alcohol, caffeine, or other substance abuse.
  • Inability to reasonably adhere to study procedures.
  • Pregnancy or breastfeeding.
  • Concurrent participation in another clinical trial.
  • Withdrawal of informed consent.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Diagnose
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Snapshot NIR Assessment

Each patient enrolled in the study will undergo the standard diagnostic and treatment process.

The only difference compared to patients not enrolled in the study will be the use of the experimental Snapshot NIR V3.0 device during the routine visits scheduled in any case, and in particular:

during the preoperative consultation between the plastic surgeon and the breast surgeon, which must take place within 30 days prior to surgery; during the pre- and post-operative phases; on the first post-operative day during hospitalization; and on the 15th (+/-5 days) post-operative day during one of the routinely scheduled dressing changes.

The Snapshot NIR V3.0 device is used to noninvasively assess superficial breast skin flap tissue oxygenation and perfusion. NIR images and tissue oxygen saturation measurements are acquired preoperatively, early postoperatively, and at a later postoperative assessment.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Tissue Oxygen Saturation (StO₂) Measured by the Snapshot NIR V3.0 Device
Zeitfenster: Baseline (preoperative), postoperative day 1, and postoperative day 15 (±5 days).
Superficial tissue oxygen saturation (StO₂, %) measured using the Snapshot NIR V3.0 imaging device. StO₂ values (%) will be obtained from predefined Regions of Interest (ROIs) identified on exported two-dimensional tissue oxygenation maps. Mean StO₂ (%) and the presence of hypoperfused areas will be evaluated at each scheduled study visit.
Baseline (preoperative), postoperative day 1, and postoperative day 15 (±5 days).
Correlation Between Snapshot NIR Tissue Oxygen Saturation (StO₂) and Clinical Assessment of Breast Skin Flap Perfusion
Zeitfenster: Baseline (preoperative), postoperative day 1, and postoperative day 15 (±5 days).
Correlation between superficial tissue oxygen saturation (StO₂, %) measured using the Snapshot NIR V3.0 device and the clinical assessment of breast skin flap perfusion performed by visual inspection. Clinical assessment findings and StO₂ measurements will be compared for the predefined Regions of Interest (ROIs). The outcome will be expressed as a correlation coefficient between StO₂ (%) measurements and the corresponding clinical assessment.
Baseline (preoperative), postoperative day 1, and postoperative day 15 (±5 days).
Temporal Change in Tissue Oxygen Saturation (StO₂) of Breast Skin Flaps
Zeitfenster: Baseline (preoperative), postoperative day 1, and postoperative day 15 (±5 days).
Change in superficial tissue oxygen saturation (StO₂, %) measured using the Snapshot NIR V3.0 device over time. Serial StO₂ measurements obtained from predefined Regions of Interest (ROIs) will be compared across study visits to evaluate the temporal evolution of tissue perfusion and hypoperfused areas.
Baseline (preoperative), postoperative day 1, and postoperative day 15 (±5 days).

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Correlation Between Snapshot NIR Tissue Oxygen Saturation (StO₂) and Intraoperative Reconstructive Strategy
Zeitfenster: Intraoperative.
Correlation between tissue oxygen saturation (StO₂, %) measured using the Snapshot NIR V3.0 device and the intraoperative reconstructive strategy selected by the surgeon (prepectoral implant versus subpectoral tissue expander). The outcome will be expressed as the correlation between StO₂ (%) measurements and the selected reconstructive strategy.
Intraoperative.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Matteo Ghilli, MD, U.O. Senologia, Azienda Ospedaliero-Universitaria Pisana (AOUP)
  • Studienstuhl: Valentina Hartwig, PhD, National Research Council, Institute of Clinical Physiology, Italy
  • Studienleiter: Maria Giovanna Trivella, MD, National Research Council, Institute of Clinical Physiology, Italy

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

10. Oktober 2024

Primärer Abschluss (Tatsächlich)

13. Februar 2026

Studienabschluss (Tatsächlich)

13. Februar 2026

Studienanmeldedaten

Zuerst eingereicht

23. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

29. Juni 2026

Zuerst gepostet (Tatsächlich)

2. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

2. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

29. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • Adisirast
  • IT-24-04-046716 (Andere Kennung: European Database on Medical Devices (EUDAMED))

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

IPD will not be shared because participants consented only to aggregated data publication and due to confidentiality and privacy constraints.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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