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RecruitingNCT07659639LASERBLOODUpdated Jun 22, 2026

Biophotonic Nanoparticle-enabled Laser Blood Test for Early Detection of Pancreatic Cancer

An interventional study of Diagnostic procedures in Diabetes, IPMN, Pancreatic and PDAC - Pancreatic Ductal Adenocarcinoma, sponsored by Fondazione Policlinico Universitario Campus Bio-Medico. Recruiting at 1 site in Italy. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-22.

Sponsored by Fondazione Policlinico Universitario Campus Bio-Medico · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
400
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

LASERBLOOD is based on a biophotonic technology that can be used to predict the development of Pancreatic Ductal Adenocarcinoma (PDAC) in particular categories of subjects at risk (e.g. persons with diabetes, obese people, patients with Intraductal Papillary Mucinous Neoplasm [IPMN] or other cystic diseases of the pancreas, etc.) and at the same time offer the possibility of verifying the real effectiveness of the treatments to which affected patients are subjected.

Read the detailed description

LASERBLOOD is based on a biophotonic technology that can be used to predict the development of Pancreatic Ductal Adenocarcinoma (PDAC) in particular categories of subjects at risk (e.g. persons with diabetes, obese people, patients with Intraductal Papillary Mucinous Neoplasm [IPMN] or other cystic diseases of the pancreas, etc.) and at the same time offer the possibility of verifying the real effectiveness of the treatments to which affected patients are subjected.

02

Conditions studied

  • Diabetes
  • IPMN, Pancreatic
  • PDAC - Pancreatic Ductal Adenocarcinoma
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

**Inclusion criteria for patients with PDAC and IPMN:**

  • No history of prior neoplastic diseases;
  • Adequate renal and hepatic function;
  • No hematologic disorders;
  • Age ≥ 18 years;
  • No active infections;
  • Written informed consent.

**Exclusion criteria:**

  • Severe pre-existing medical conditions, such as serious illnesses or other medical conditions that could negatively affect study outcomes or pose a high risk to the patient's health;
  • Ongoing therapies that could interfere with the study or alter the results.
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
400 participants (estimated)

Study arms

  • Experimental
    DIAGNOSTIC

    Acquisition of biological material for bio-photonic technology analysis

    Diagnostic Test: Diagnostic procedures

Interventions

  • Diagnostic testDiagnostic procedures

    Acquisition of biological material for bio-photonic technology analysis

05

What researchers measure

Primary outcomes

  1. Diagnostic Accuracy of the Biophotonic Nanoparticle-Enabled Laser Blood Test (LASERBLOOD) for Detection of Pancreatic Ductal Adenocarcinoma (PDAC)

    Area Under the Receiver Operating Characteristic Curve (AUC-ROC), with 95% confidence interval, of fluorescence lifetime fingerprints obtained by biophotonic laser analysis of nanoparticle-protein corona complexes in plasma, in discriminating subjects with histologically confirmed Pancreatic Ductal Adenocarcinoma (PDAC) from subjects without PDAC (including healthy controls and patients with Intraductal Papillary Mucinous Neoplasm \[IPMN\]). The reference standard is histopathological diagnosis (on surgical specimen or endoscopic ultrasound-guided fine-needle aspiration/biopsy \[EUS-FNA/B\]) for PDAC and IPMN, and radiological/clinical assessment for healthy controls.

    Time frame: At baseline (time of enrollment), with reference standard diagnosis confirmed within 12 months

Secondary outcomes

  1. Sensitivity and Specificity of Fluorescence Lifetime (FL) Fingerprints for Pancreatic Ductal Adenocarcinoma (PDAC) Detection at Optimal Cut-off

    Sensitivity and specificity (percentage, with 95% confidence intervals) of fluorescence lifetime fingerprints in discriminating subjects with PDAC from subjects without PDAC, calculated at the optimal cut-off value determined by Youden's J index from the ROC analysis. Reference standard: histopathological diagnosis (surgical specimen or EUS-FNA/B) for PDAC and IPMN, radiological/clinical assessment for healthy controls.

    Time frame: At baseline (time of enrollment), with reference standard diagnosis confirmed within 12 months

  2. Correlation Between Fluorescence Lifetime (FL) Fingerprints and Clinical Stage of Pancreatic Ductal Adenocarcinoma (PDAC)

    Spearman correlation coefficient (ρ), with 95% confidence interval, between fluorescence lifetime fingerprint values and clinical stage of PDAC at diagnosis, classified according to the 8th edition American Joint Committee on Cancer (AJCC) TNM staging system (Stage I-II: early disease; Stage III-IV: advanced disease).

    Time frame: At time of PDAC diagnosis (within 12 months from enrollment)

  3. Mean Fluorescence Lifetime (FL) Values of Nanoparticle-Protein Corona Complexes in Plasma Samples, by Diagnostic Group

    Mean fluorescence lifetime values, in nanoseconds (ns), measured by biophotonic laser analysis of plasma samples incubated with nanoparticles, reported as mean ± standard deviation (SD) separately for each diagnostic group: Pancreatic Ductal Adenocarcinoma (PDAC), Intraductal Papillary Mucinous Neoplasm (IPMN), and healthy controls.

    Time frame: At baseline (time of enrollment), prior to any treatment

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Study locations

1 of 1 sites recruiting
  • Fondazione Policlinico Universitario Campus Bio-Medico
    Rome, Italy 00128, Italy
    Recruiting
07

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07659639
Lead sponsor
Fondazione Policlinico Universitario Campus Bio-Medico
Responsible party
Sponsor
First posted
Jun 22, 2026
Start date
Sep 1, 2025
Primary completion
Aug 2029 (estimated)
Completion
Aug 2029 (estimated)
Last update
Jun 22, 2026

Study contacts

Damiano Caputo, MD
Contact
d.caputo@policlinicocampus.it
+3906225418012

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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