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Improving Outcomes of Respiratory Patients With Exertional Hypoxemia

C

Changi General Hospital

Status

Enrolling

Conditions

Pulmonary Rehabilitation

Treatments

Device: High flow oxygen
Other: Usual care

Study type

Interventional

Funder types

Other

Identifiers

NCT05752370
2022/2605

Details and patient eligibility

About

The primary aim of this pilot randomized controlled trial is to determine feasibility of the proposed pulmonary rehabilitation intervention.

Full description

In this pilot randomized controlled trial, our primary aim is to determine feasibility of the proposed intervention.

Enrollment

56 estimated patients

Sex

All

Ages

21 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 21 years and above
  • Presence of exertional hypoxemia during 1-minute sit-to-stand test
  • diagnosis of acute COPD exacerbation or Covid-19 pneumonia or exacerbation of bronchiectasis or exacerbation of interstitial lung disease
  • physically fit to participate in exercise therapy as determined by both the patient's physician and physiotherapist

Exclusion criteria

  • uncontrolled severe medical conditions
  • currently enrolled in a pulmonary rehabilitation trial
  • unsuitable for randomization as determined by the patient's physician

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

56 participants in 2 patient groups

High flow oxygen
Experimental group
Description:
High flow nasal oxygen
Treatment:
Device: High flow oxygen
Usual care
Active Comparator group
Description:
room air or normal flow oxygen
Treatment:
Other: Usual care

Trial contacts and locations

1

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Central trial contact

Yingjuan Mok, MBBS

Data sourced from clinicaltrials.gov

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