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NCT04490369

Evaluation of Pain and Discomfort in the Cardiac Catheterization Lab

Completed Last updated 3 February 2023
What this trial tests

trial in Patient Comfort in 175 participants. Completed in 30 April 2021.

Timeline
7 December 2020
Primary endpoint
30 April 2021
30 April 2021

Quick facts

Lead sponsorDuke University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment175
Start date7 December 2020
Primary completion30 April 2021
Estimated completion30 April 2021
Sites1 location across United States

Conditions studied

Sponsor

Duke University

Who can join

18 and older, any sex, with Patient Comfort. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to explore how the timing of procedural sedation medications influences patient comfort and satisfaction with sedation. Participation in this study will included be randomly assigned to one of two groups (long and short) within standard of care. Each group will observe a time interval between receiving procedural sedation medications and the start of the procedure. A trained observer will evaluate patient experience during the procedure and at the end of the procedure we will ask the participant 3 brief questions about the experience. All other information collected about the experience during the procedure will occur as part of usual care. No further activities will be asked as part of this study. All study activities will occur during a scheduled visit and participation is complete once questions have been answered.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Duke University 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/NCT04490369.

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