- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06266117
Pain, Anxiety, and Comfort Levels in Coronary Angiography
Investigation of Factors Affecting Pain, Anxiety, and Comfort Levels in Patients Undergoing Coronary Angiography
Study Overview
Status
Conditions
Detailed Description
In the first part, the descriptive information of the patients will be used, and in the second part, "Perianesthesia Comfort Scale", "State/Trait Anxiety Scale" and "General Comfort Scale (GAS)" adapted into Turkish by Üstündağ and Aslan in 2010 will be used. Visual Pain Scale will be used for pain measurement.
It is planned that the data for the Perianesthesia Comfort Scale (PCI) will be collected in the patient's room on the first postoperative day, in approximately 15 minutes, by face-to-face interview method.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Muhammed Nur ÖGÜN
- Phone Number: 090 374 253 46 56
- Email: muhammed.ogun@ibu.edu.tr
Study Locations
-
-
Merkez
-
Bolu, Merkez, Turkey, 14100
- Abant Izzet Baysal University Faculty of Health Science
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- over 18 years Conscious patients
Exclusion Criteria:
- Patients undergoing intubation
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain level
Time Frame: on the 1st postoperative days
|
Visual Pain Scale
|
on the 1st postoperative days
|
Anxiety
Time Frame: on the 1st postoperative days
|
State/Trait Anxiety Scale
|
on the 1st postoperative days
|
Comfort
Time Frame: on the 1st postoperative days
|
Perianesthesia Comfort Scale
|
on the 1st postoperative days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SBF-HMS-GES-03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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