Cystic Fibrosis (CF) Flow Rates Study

Syntara

Status: Completed

Conditions: Cystic Fibrosis

Study type: Observational

Funder types: Industry

Identifiers

NCT00779077

DPM-OSM-403

Details and patient eligibility

About

We wish to measure the inspiratory flow and volumes generated by the subjects inhaling from a spirometer with a high resistance dry powder inhaler in series in subjects with cystic fibrosis.

Enrollment: 25 patients

Sex: All

Ages: 6 to 50 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• CF
• FEV1 ≥ 30% and < 90% predicted

Exclusion criteria

• Be considered "terminally ill" or listed for lung transplantation
• Have had a lung transplant
• Have had a significant episode of haemoptysis (>60 ml) in the three months prior to enrolment
• Have had a myocardial infarction in the three months prior to enrolment
• Have had a cerebral vascular accident in the three months prior to enrolment
• Have had major ocular surgery in the three months prior to enrolment
• Have had major abdominal, chest or brain surgery in the three months prior to enrolment
• Have a known cerebral, aortic or abdominal aneurysm
• Be breast feeding or pregnant
• Be using beta blockers
• Have unstable asthma

Trial design

25 participants in 1 patient group

cystic fibrosis

Description:

adults and children with cystic fibrosis