Bottle PEP in Cystic Fibrosis

Safety and Sustainability in Bottle PEP in Cystic Fibrosis

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04961008

Enrollment

Registered

2021-07-14

Start date

2019-04-01

Completion date

2020-10-31

Last updated

2021-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

Brief summary

The study aims to investigate the sustainability of Bottle-PEP in patients with cystic fibrosis

Interventions

OTHERBottle-PEP

A device that gives positive pressure from a bottle with the help of a non deflating tube

OTHERRoutine physiotherapy

Routine pulmonary physiotherapy

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

6 Years to 18 Years

Healthy volunteers

Inclusion criteria

* Diagnosis of cystic fibrosis * Acute exacerbation

Exclusion criteria

* Any contraindication using the Bottle - PEP such as the presence of pneumothorax

Design outcomes

Primary

Measure	Time frame	Description
6 minute walk test	every 3 months	distance of meters walked in 6 minutes

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026