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NCT00951886 Clinical Trial

The Validity of Forced Expiratory Maneuvers in Ataxia Telangiectasia Studied Longitudinally

Ataxia Telangiectasia Clinical Trial

Official title:
The Validity of Forced Expiratory Maneuvers in Ataxia Teleangiectasia Studied Longitudinally

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00951886
Other study ID # SHEBA-08-5418-OE-CTIL
Secondary ID
Status Active, not recruiting
Phase N/A
First received August 2, 2009
Last updated August 3, 2009
Start date July 2009
Est. completion date July 2009

Study information
Verified date August 2009
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

Rationale: Forced spirometry maneuvers are not routinely performed in patients with Ataxia Telangiectasia (A-T), even though they suffer from respiratory illnesses.

Objectives: To study the feasibility and validity of forced spirometry in A-T patients.

Methods: Patients will perform spirometry during clinical visits. Parameters studied will be technical quality, relation to predicted values, age, pulmonary illness, body mass index, mutational status and mutation.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 28
Est. completion date July 2009
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 3 Years to 20 Years
Eligibility Inclusion Criteria:

- Patients with proven Ataxia Telangiectasia

Exclusion Criteria:

- inability to perform spirometry

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Pediatric Pulmonary Unit, The Edmond and Lily Safra Children's Hospital Chaim Sheba Medical Center, Tel HaShomer Ramat-Gan

Sponsors (1)
Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary spirometry measurements 3 years No
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