Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04618302
Other study ID # 2020-01756
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 19, 2020
Est. completion date January 1, 2021

Study information

Verified date April 2021
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study investigates the test-retest reliability of the lung diffusing capacity for nitric oxide in healthy individuals during exercise.


Description:

The aim of this study of to evaluate the test-retest reliability of single-breath lung diffusing capacity measurements for nitric oxide (DLNO) in healthy individuals during light and moderate intensity cycling exercise. Healthy subjects will perform repeated single-breath DLNO measurements during light (i.e., at 50% of the first ventilatory threshold) and moderate intensity exercise (i.e., 80% of the first ventilatory threshold) on a stationary cycle ergometer.


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date January 1, 2021
Est. primary completion date December 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Healthy - Age 18 yrs and older - Ability to follow study procedures and instructions in German Exclusion Criteria: - Any known cardiopulmonary or metabolic diseases (e.g., heart disease, diabetes mellitus etc) - Obesity (BMI > 30kg/m2) - Smoking (ex-smoker allowed; if they stopped smoking at least one year before the examination) - Mental impairment leading to inability to cooperate - Respiratory infection in the last two weeks - Forced expiratory volume in 1s/ forced vital capacity (FEV1/FVC ratio) FEV1/FVC ratio < lower limit of normal according to equations by Quanjer et al. Eur Respir J 2012.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland University of Zurich and University Hospital of Zurich Zurich

Sponsors (1)

Lead Sponsor Collaborator
Thomas Radtke

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diffusing capacity for nitric oxide (DLNO) DLNO (in ml/min/mmHg) measured at 80% of the gas exchange threshold during cycling exercise. At second study visit
Primary Diffusing capacity for nitric oxide (DLNO) DLNO (in ml/min/mmHg) measured at 80% of the gas exchange threshold during cycling exercise. At third study visit, approximately 1-2 weeks after second study visit
Secondary Diffusing capacity for nitric oxide (DLNO) DLNO (in ml/min/mmHg) measured at 50% of the gas exchange threshold during cycling exercise. At second study visit
Secondary Diffusing capacity for nitric oxide (DLNO) DLNO (in ml/min/mmHg) measured at 50% of the gas exchange threshold during cycling exercise. At third study visit, approximately 1-2 weeks after second study visit
Secondary Diffusing capacity for carbon monoxide (DLCO) DLCO (in ml/min/mmHg) measured at 50% of the gas exchange threshold during cycling exercise. At second study visit
Secondary Diffusing capacity for carbon monoxide (DLCO) DLCO (in ml/min/mmHg) measured at 50% of the gas exchange threshold during cycling exercise. At third study visit, approximately 1-2 weeks after second study visit
Secondary Diffusing capacity for carbon monoxide (DLCO) Agreement in DLCO (in ml/min/mmHg) measured at 80% of the gas exchange threshold during cycling exercise. At second study visit
Secondary Diffusing capacity for carbon monoxide (DLCO) Agreement in DLCO (in ml/min/mmHg) measured at 80% of the gas exchange threshold during cycling exercise. At third study visit, approximately 1-2 weeks after second study visit
Secondary Alveolar volume (VA) VA (in L) measured at 50% of the gas exchange threshold during cycling exercise. At second study visit
Secondary Alveolar volume (VA) VA (in L) measured at 50% of the gas exchange threshold during cycling exercise. At third study visit, approximately 1-2 weeks after second study visit
Secondary Alveolar volume (VA) Alveolar volume (in L) measured at 80% of the gas exchange threshold during cycling exercise. At second study visit
Secondary Alveolar volume (VA) Alveolar volume (in L) measured at 80% of the gas exchange threshold during cycling exercise. At third study visit, approximately 1-2 weeks after second study visit
Secondary Breath hold time (BHT) BHT (in s) measured at 80% of the gas exchange threshold during cycling exercise. At second study visit
Secondary Breath hold time (BHT) BHT (in s) measured at 80% of the gas exchange threshold during cycling exercise. At third study visit, approximately 1-2 weeks after second study visit
Secondary Breath hold time (BHT) BHT (in s) measured at 50% of the gas exchange threshold during cycling exercise. At second study visit
Secondary Breath hold time (BHT) BHT (in s) measured at 50% of the gas exchange threshold during cycling exercise. At third study visit, approximately 1-2 weeks after second study visit
See also
  Status Clinical Trial Phase
Recruiting NCT06052553 - A Study of TopSpin360 Training Device N/A
Completed NCT05511077 - Biomarkers of Oat Product Intake: The BiOAT Marker Study N/A
Recruiting NCT04632485 - Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
Completed NCT05931237 - Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults N/A
Terminated NCT04556032 - Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women N/A
Completed NCT04527718 - Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers Phase 1
Completed NCT04998695 - Health Effects of Consuming Olive Pomace Oil N/A
Completed NCT04107441 - AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects Phase 1
Completed NCT04065295 - A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225 Phase 1
Completed NCT01442831 - Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects Phase 1
Terminated NCT05934942 - A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood Phase 1
Recruiting NCT05525845 - Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI N/A
Completed NCT05515328 - A Study in Healthy Men to Test How BI 685509 is Processed in the Body Phase 1
Completed NCT05030857 - Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects Phase 1
Completed NCT04967157 - Cognitive Effects of Citicoline on Attention in Healthy Men and Women N/A
Recruiting NCT04494269 - A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls Phase 1
Recruiting NCT04714294 - Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers Phase 1
Completed NCT04539756 - Writing Activities and Emotions N/A
Recruiting NCT04098510 - Concentration of MitoQ in Human Skeletal Muscle N/A
Completed NCT03308110 - Bioavailability and Food Effect Study of Two Formulations of PF-06650833 Phase 1