Skip to main content
Clinical Trials/CTIS2023-503686-26-00
CTIS2023-503686-26-00Active, not recruitingPhase 1

PET/CT imaging with FAPI as a biomarker for the distinction between predominant active fibrotic and inflammatory phenotypes in patients with progressive pulmonary fibrosis: The FIBRO-PET study.

St Antonius Hospital0 sites20 target enrollmentStarted: November 10, 2023Last updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Active, not recruiting
Enrollment
20

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 65+ (—)
Sex
All

Inclusion Criteria

  • = 18 years of age, New diagnosis of PPF, A minimum of 20% of lung parenchyma is aberrant (fibrosis, inflammation or both), MDT indication for treatment with either immunosuppressive drugs or antifibrotic drug

Exclusion Criteria

  • Prior or current treatment with antifibrotic drugs, Active malignancy, Inability to undergo a PET/CT at the Sint Antonius Hospital, Incapacity to give informed consent personally, Pregnancy

Investigators

Similar Trials

Not yet recruiting
Not Applicable
The diagnostic value of FAPI PET/CT in staging of newly diagnosed PCa10038597Prostate cancer
NL-OMON53628Antoni van Leeuwenhoek Ziekenhuis30
Recruiting
Unknown
Pathophysiological assessment by FAPI-PET targeting cancer-associated fibroblasts in proton therapyCancer
JPRN-UMIN000052534Southern Tohoku Research Institute for Neuroscience80
Unknown
Not Applicable
Visualized Monitoring of Fibrosis Formation in Heart Failure With 68GA-FAPI PETPositron Emission TomographyHeart Failure
NCT04982458Wuhan Union Hospital, China50
Active, not recruiting
Phase 1
The use of FES-PET imaging as a tool to detect a possible reversion of Estrogen Receptor (ER)-a status in patients with metastatic breast cancer HER2 + and ERa neg treated with trastuzumab + pertuzumab + taxane.Metastatic breast cancer HER2 + and ERa neg.MedDRA version: 20.0Level: LLTClassification code 10027475Term: Metastatic breast cancerSystem Organ Class: 100000004864
EUCTR2018-001552-36-FRINSTITUT CLAUDIUS REGAUD33
Active, not recruiting
Phase 1
A bone scan in combination with some specific blood samples for the classification of bone disease in patients suffering from chronic kidney disease.Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD), especially renal osteodystofi.MedDRA version: 20.0 Level: LLT Classification code 10065404 Term: Combined positron emission tomogram and computerised tomogram System Organ Class: 10022891 - InvestigationsMedDRA version: 20.0 Level: SOC Classification code 10022891 Term: Investigations System Organ Class: 10022891 - InvestigationsMedDRA version: 20.0 Level: LLT Classification code 10066622 Term: Chronic hemodialysis System Organ Class: 100000004865
EUCTR2016-005160-34-DKniversitetsklinikken for Nyresygdomme og Blodtryksforhøjelse, Regionshospitalet Holstebro, Hospitalsenheden Vest40