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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02382237
Other study ID # ICM2013/31
Secondary ID
Status Completed
Phase N/A
First received February 4, 2014
Last updated August 16, 2017
Start date October 2013
Est. completion date August 9, 2017

Study information

Verified date August 2017
Source Institut du Cancer de Montpellier - Val d'Aurelle
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluate the feasability to determine the difference of tumoral metabolism before and after artificial nutrition.


Description:

Evaluation of the feasability to determine the difference of tumoral metabolism before and after artificial nutrition. This activity will be measured with TEP/TDM 18F-FDG


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 9, 2017
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- VADS cancer or oesophageal cancer

- Evaluation by 18F-FDG PET

- denutrition with weight loss of 5%

- Artificial nutrition

- ECOG<2

Exclusion Criteria:

- Treatment by chemotherapy, surgery unless 2 months

- Treatment by radiotherapy unless 4 months

- Capillar glycemia >12mmol/l during the PET

Study Design


Intervention

Device:
PET/TDM
Evaluation of nutrition absorption by TEP/TDM

Locations

Country Name City State
France ICM Val d'Aurelle Montpellier

Sponsors (1)

Lead Sponsor Collaborator
Institut du Cancer de Montpellier - Val d'Aurelle

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary rate of Standardized Uptake Value (SUV) The variation of the SUVmax is defined as the difference of the tumoral SUV max between the TEP1 and the TEP2 3 months
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