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Time to Perform Lung Function Test in Cystic Fibrosis

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01737801
First Posted: November 30, 2012
Last Update Posted: November 30, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Cecilia Rodriguez, Karolinska University Hospital
  Purpose

Time to perform lung function test after chest physiotherapy in cystic fibrosis.

The investigators study FEV1(forced expiratory volume in one second) and FVC (forced vital capacity).


Condition Intervention
Cystic Fibrosis Procedure: Lung function test

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Time to Perform Lung Function Test in Cystic Fibrosis After Chest Physiotherapy.

Resource links provided by NLM:


Further study details as provided by Cecilia Rodriguez, Karolinska University Hospital:

Primary Outcome Measures:
  • Lung function test. FEV1 and FVC [ Time Frame: 2 days ]

Enrollment: 24
Study Start Date: February 2008
Study Completion Date: September 2012
Primary Completion Date: January 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Lung function test
Lung function test
Procedure: Lung function test
Lung function test.
Other Name: Lung function test.

Detailed Description:
The patients perform spirometry before, direct after, 30 minutes, 1 hour, 2 hours, and 3 hours after physiotherapist. The investigators want to study the FEV1 and FVC.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   5 Years to 80 Years   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients with cystic fibrosis

Exclusion Criteria:

  • patients with cystic fibrosis who could not stay at the clinic for more than 4 hrs.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01737801


Locations
Sweden
Karolinska University Hospital
Stockholm, Sweden
Sponsors and Collaborators
Karolinska University Hospital
Investigators
Principal Investigator: Cecilia Rodriguez, Physio Karolinska Institutet
  More Information

Responsible Party: Cecilia Rodriguez, Physiotherapist, Karolinska University Hospital
ClinicalTrials.gov Identifier: NCT01737801     History of Changes
Other Study ID Numbers: 2012-CF-2
First Submitted: November 19, 2012
First Posted: November 30, 2012
Last Update Posted: November 30, 2012
Last Verified: November 2012

Keywords provided by Cecilia Rodriguez, Karolinska University Hospital:
Lung function
Physiotherapy

Additional relevant MeSH terms:
Fibrosis
Cystic Fibrosis
Pathologic Processes
Pancreatic Diseases
Digestive System Diseases
Lung Diseases
Respiratory Tract Diseases
Genetic Diseases, Inborn
Infant, Newborn, Diseases