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The Effectiveness of BreatheMAX Breathing Device on Secretion Clearance (ESMOSC)

K

Khon Kaen University

Status and phase

Unknown
Phase 3
Phase 2

Conditions

Lung Disease

Treatments

Device: BreatheMAX breathing device

Study type

Interventional

Funder types

Other

Identifiers

NCT01090804
47660279

Details and patient eligibility

About

The purpose of this study is to determined effects of BreatheMAX on secretion clearance.

Enrollment

14 estimated patients

Sex

All

Ages

15 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • One sign of secretion accumulation in bronchi
  • Stable cardiopulmonary function
  • Good consciousness and good co-operation

Exclusion criteria

  • Massive hemoptysis
  • Pneumothorax (untreated)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

14 participants in 1 patient group

breathing exercise
Experimental group
Description:
BreatheMAX breathing device is Water pressure Threshold Bottle. The level of water in the cylinder determines the load for treatment. In the treatment using 20% PNIP (Peak negative inspiratory pressure) was performed with 6-10 breaths/set; 10 set/day
Treatment:
Device: BreatheMAX breathing device

Trial contacts and locations

1

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Central trial contact

Miss Sujittra Kluayhomthong, Bachelor; Mrs. Chulee Jones, Philosophy

Data sourced from clinicaltrials.gov

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