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NCT02499666: EXERTION

Change in Exercise Capacity as Measured by Peak Oxygen Uptake After CTO PCI

Terminated Last updated 7 March 2022
What this trial tests

trial testing Percutaneous Coronary Intervention in Coronary Artery Disease in 15 participants. Terminated before completion.

Timeline
29 June 2015
Primary endpoint
30 October 2017
30 October 2017

Quick facts

Lead sponsorHenry Ford Health System
StatusTerminated
Study typeOBSERVATIONAL
Enrollment15
Start date29 June 2015
Primary completion30 October 2017
Estimated completion30 October 2017
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Henry Ford Health System — full company profile →

Who can join

Adults 18 to 90, any sex, with Coronary Artery Disease or Angina Pectoris. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this project is to objectively assess the change (improvement) in exercise capacity in patients undergoing routine percutaneous coronary intervention (PCI) for chronic total occlusion (CTO)

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Percutaneous Coronary Intervention

Trials testing the same drug.

Other recruiting trials for Coronary Artery Disease

Currently open trials in the same condition.

Other Henry Ford Health System trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02499666.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing