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Evaluation of Pain and Discomfort in the Cardiac Catheterization Lab

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Duke University

Status

Completed

Conditions

Patient Comfort

Study type

Observational

Funder types

Other

Identifiers

NCT04490369
Pro00102686

Details and patient eligibility

About

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.

Enrollment

175 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • English speaking
  • Coming to Duke University for Cardiac Catheterization

Exclusion criteria

Trial design

175 participants in 2 patient groups

Group 1- short interval
Description:
Less than or equal to six minutes between receiving sedation and the start of the procedure
Group 2- long interval
Description:
Greater than or equal to seven minutes between receiving sedation and the start of the procedure

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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