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NCT02078141
18F-deoxyglucose (FDG) PET-CMD
NA trial testing 18F-deoxyglucose (FDG) in Patients With Idiopathic Dilated Cardiomyopathy in 30 participants. Completed in 18 January 2018.
18 January 2018
Quick facts
| Lead sponsor | Nantes University Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | diagnostic |
| Enrollment | 30 |
| Start date | 24 June 2014 |
| Primary completion | 18 January 2018 |
| Estimated completion | 18 January 2018 |
| Sites | 2 locations across France |
Drugs / interventions tested
- 18F-deoxyglucose (FDG) — full drug profile →
Conditions studied
- Patients With Idiopathic Dilated Cardiomyopathy — all drugs for Patients With Idiopathic Dilated Cardiomyopathy →
Sponsor
Nantes University Hospital
Who can join
18 and older, any sex, with Patients With Idiopathic Dilated Cardiomyopathy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) may have application in a promising tool for identification of myocardial inflammation in patients with dilated cardiomyopathy (DCM).Therefore, the purpose of the study is to confirm the hypothesis of the fixation of FDG in non cardiomyocyte cells in a number of patients with DCM, to specify the frequency and describe the different binding profiles in comparison with MRI data. Patients will perform an ethologic evaluation of a non ischemic DCM with in a cardiac MRI. All patients will have with in 4 weeks after the MRI a 18F-fluorodeoxyglucose (FDG) PET. A high fat and low carbohydrate diet and an heparin injection will be prescribed to patients before this FDG PET. Patients will be identified as FDG+ or FDG -. The clinical status of the patient will be completed by a 12 months evaluation.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT02078141
- Europe PMC full search
- ASCO Meeting Library
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02078141 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Nantes University Hospital
- Last refreshed: 26 July 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02078141.
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