Clinical Trials Directory

Trials / Unknown

UnknownNCT06027372

Heart Rate Variability and Nocturnal Blood Oxygen Saturation in Patients With Idiopathic Pulmonary Fibrosis

Differences in Heart Rate Variability and Nocturnal Blood Oxygen Saturation of Patients With Idiopathic Pulmonary Fibrosis Between at Baseline and During Acute Exacerbation

Status
Unknown
Phase
Study type
Observational
Enrollment
70 (estimated)
Sponsor
Taipei Veterans General Hospital, Taiwan · Other Government
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

The goal of this observational study is to compare the overnight heart rate variability (HRV) and nocturnal oxygen saturation (SpO2) in patients with idiopathic pulmonary fibrosis (IPF). The main questions it aims to answer are: (1). if there are correlations between pulmonary function test and HRV and overnight SpO2; (2). if HRV and SpO2 can predict the occurrence of acute exacerbation in patients with IPF. Participants will be asked to examine pulmonary function test (including lung volumes and six-minute walk test) and wear pulse oxygenation recorder and "LARGAN" ECG Holter" ("LARGAN HEALTH TECHNOLOGY" Sleep Apnea And Sleep Quality Examination System) during sleep.

Conditions

Interventions

TypeNameDescription
DEVICE"LARGAN" ECG Holterwear "LARGAN" ECG Holter during sleep once after completion of pulmonary function test

Timeline

Start date
2020-05-21
Primary completion
2023-08-27
Completion
2024-06-30
First posted
2023-09-07
Last updated
2023-09-07

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT06027372. Inclusion in this directory is not an endorsement.