Development and Validation of a Disease Specific PROM to Assess Abdominal Involvement in Patients With CF (CFAbd-Score)

Recruiting Observational Study
Cystic Fibrosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Sex
Any
Study type
Observational
Participants needed
2,000 (estimated)
Sponsor
Medizinische Hochschule Brandenburg Theodor Fontane · Other
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About This Trial
Development, validation and evaluation of a new multimodal questionnaire to assess and quantify the abdominal involvement in patients with the inherited life shortening multi-organ disease Cystic fibrosis. In the stepwhise development of the patient reported outcome measures (PROM) repeadedly, CF-patients, their families as well as professionals working in different fields of CF-care will be incl…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: CF cohort: Diagnosis of CF determined by * a sweat chloride of \>60 mEq/L and/or * detection of 2 disease causing CFTR mutations with evidence of organ involvement. Healthy controls: * Age-matched Exclusion Criteria: CF cohort: * Lacking ability to cooperate of patients /…
Contacts

Jochen G Mainz, Prof. MD

+493381411803

jochen.mainz@mhb-fontane.de

CONTACT

Franziska Duckstein, MA

+493381411841

f.duckstein@klinikum-brandenburg.de

CONTACT