Skip to main content
Clinical Trials/NCT02892981
NCT02892981CompletedNot Applicable

Dead Space Evaluation During Exercise in Patients With Pulmonary Hypertension

Centro Cardiologico Monzino0 sites18 target enrollmentStarted: January 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
18
Primary Endpoint
dead space ventilation (measured in L/min)

Study Overview

Brief Summary

Aim of the study is to evaluate the role of chemoreceptor activity and ventilation perfusion mismatch on the genesis of exercise induced hyperventilation in Pulmonary hypertension patients. So the investigators tested the chemoreceptor response at rest, both with hypoxic and hypercapnic stimuli, and the ventilatory response during exercise analyzing its two components, alveolar and dead space ventilation.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •age ≥18 and ≤ 80 years
  • •ability to understand the research protocol and willing to sign the study informed consent
  • •diagnosis of pulmonary arterial hypertension belonging to Class I and IV
  • •stable haemodynamic status and optimized medical treatment since at least 2 months
  • •ability to perform maximal cardiopulmonary exercise test and pulmonary diffusing capacity for carbon monoxide evaluation

Exclusion Criteria

  • •relevant comorbidities
  • •usual contraindications for cardiopulmonary exercise test
  • •pulmonary hypertension associated to left heart and pulmonary disease, congenital heart diseases with evident cardiac shunts.

Arms & Interventions

Pulmonary hypertension patients

Other

All Pulmonary hypertension patients enrolled in the study underwent a cardiopulmonary exercise test and hypoxia and hypercapnia tests

Intervention: cardiopulmonary exercise test,hypoxia and hypercapnia test (Other)

Outcomes

Primary Outcomes

dead space ventilation (measured in L/min)

Time Frame: 1 week

Dead space ventilation is calculated through the equation: VT\* \[1- (863\*VCO2)/(VE\*PaCO2)\], where VT = tidal volume, VCO2= CO2 output, VE= pulmonary ventilation,PaCO2 is the arterial partial pressure of CO2 and 863 is a constant.

Secondary Outcomes

  • central hypercapnic chemosensitivity (measured in L/min/mmHg)(1 week)
  • peripheral response to hypoxia (measured in L/min/O2)(1 week)
  • peripheral response to hypercapnia (measured in L/min/mmHg)(1 week)

Investigators

Sponsor
Centro Cardiologico Monzino
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Piergiuseppe Agostoni

Professor

Centro Cardiologico Monzino

Similar Trials