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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01818193
Other study ID # 2011/60
Secondary ID
Status Terminated
Phase N/A
First received March 13, 2013
Last updated October 28, 2016
Start date June 2012
Est. completion date March 2014

Study information

Verified date October 2016
Source Hopital Foch
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Observational

Clinical Trial Summary

A monocentric prospective open study to evaluate the frequency and nature of cognitive complications in the 3rd month post pulmonary transplant.


Recruitment information / eligibility

Status Terminated
Enrollment 28
Est. completion date March 2014
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients more than 18 years of age.

- Enregistered in lung transplant waiting list

- Have given their agreement to be enrolled in the study

Exclusion Criteria:

- Patients had a previous lung transplant

- patients with insufficient level of french language that may affect the comprehension and answering the psychometric test

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Hôpital FOCH Suresnes Ile de France

Sponsors (1)

Lead Sponsor Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rey auditory verbal learning test 3 months No
Primary Rey complex figure test 3 months No
Primary Boston naming test of 30 figures 3 months No
Primary Visual construction skills 3 months No
Primary Grooved Pegboard test 3 months No