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Weaning Protocol for High Flow Nasal Cannula Oxygen Therapy (SLOWH)

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Seoul National University

Status

Completed

Conditions

Respiratory Insufficiency
High Flow Nasal Cannula

Treatments

Device: FiO2 reduction first
Device: Flow reduction first
Device: Simultaneous (flow and FiO2) reduction

Study type

Interventional

Funder types

Other

Identifiers

NCT03845244
B-1809-492-006

Details and patient eligibility

About

High flow nasal cannula oxygen therapy has been widely used in critically ill patients. Despite effectiveness of high flow nasal cannula as a treatment, optimal methods to withdrawal high flow nasal cannula after recovery from preexisting conditions has not been investigated to date. In this study, we will evaluate the efficacy and safety of three different weaning methods in patients with high flow nasal cannula oxygen therapy.

Full description

Comparison of three weaning strategies: flow reduction first versus fraction of inspired oxygen (FiO2) first versus simultaneous reduction

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patients applying high flow nasal cannula and satisfying the following weaning criteria.

    1. Patient who has recovered from the underlying condition
    2. No signs of respiratory distress like agitation, diaphoresis or anxiety
    3. Arterial pH ≥ 7.35, SpO2 > 90% on FiO2 ≤ 0.5
    4. Respiratory rate ≤ 25/min, Heart rate ≤120/min, Systolic blood pressure ≥ 90mmHg

Exclusion criteria

  • Severe hypercapnia (pH <7.25)
  • Respiratory arrest requiring tracheal intubation
  • Cardiac arrest, acute coronary syndrome or life threatening arrhythmias
  • Failure of more than two organs
  • Recent trauma or burns of the neck and face
  • Non- cooperation
  • Pregnancy
  • Refusal of treatment

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 3 patient groups

Flow reduction first group
Active Comparator group
Description:
Flow reduction first -\> FiO2 reduction -\> conventional oxygen therapy
Treatment:
Device: Flow reduction first
FiO2 reduction first group
Active Comparator group
Description:
FiO2 reduction first -\> flow reduction -\> conventional oxygen therapy
Treatment:
Device: FiO2 reduction first
Simultaneous reduction group
Active Comparator group
Description:
Simultaneous (Flow and FiO2) reduction -\> conventional oxygen therapy
Treatment:
Device: Simultaneous (flow and FiO2) reduction

Trial contacts and locations

1

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Central trial contact

Eun Sun Kim, MD

Data sourced from clinicaltrials.gov

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