- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03768102
Comparison of Verbal Rating Scale and Numerical Rating Scale in Post Anesthesia Care Unit
October 19, 2020 updated by: Jin-Tae Kim, Seoul National University Hospital
Comparative Study of Verbal Rating Scale and Numerical Rating Scale in Post Anesthesia Care Unit
In the postanesthetic care unit(PACU), patients who are recovering from anesthesia are not easy to communicate with.
Accordingly, accurate evaluation of acute surgical pain is difficult for PACU patients in spite of severe postoperative pain.
Therefore, pain evaluation is clinically important and challenging in PACU.
The pain evaluation tool should be simple and easy to understand for accurate assessment.
Among the most commonly used pain assessment methods are numerical rating scale(NRS), visual analogue scale(VAS) and verbal rating scale(VRS).
These three methods have proved valid for clinical situations in many studies.
VRS appears to be easier to understand than the other two methods for patients in PACU.
The purpose of this study is to compare NRS and VRS in PACU patients.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Select
-
Seoul, Select, Korea, Republic of, 110-744
- Jin-Tae Kim
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
An adult patient who has been transferred to the recovery room after receiving general anesthesia
Description
Inclusion Criteria:
- Adult patients who underwent general anesthesia
- The American Society of Anesthesiologists(ASA) physical status classification system : class 1, 2, 3
Exclusion Criteria:
- The American Society of Anesthesiologists(ASA) physical status classification system : class 4, 5
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain measurement by the numerical rating scale
Time Frame: 5 minutes after transferred into the postanesthesia care unit
|
Patients verbally requested to rate their pain : "Rate your pain from 0 (no pain) to 10 (unbearable pain)". 0 point is the minimum and 10 point is the maximum. The higher the score, the more severe the pain. |
5 minutes after transferred into the postanesthesia care unit
|
|
Pain measurement by the numerical rating scale
Time Frame: 20 minutes after transferred into the postanesthesia care unit
|
Patients verbally requested to rate their pain : "Rate your pain from 0 (no pain) to 10 (unbearable pain)" 0 point is the minimum and 10 point is the maximum.
The higher the score, the more severe the pain.
|
20 minutes after transferred into the postanesthesia care unit
|
|
Pain measurement by the numerical rating scale
Time Frame: 40 minutes after transferred into the postanesthesia care unit
|
Patients verbally requested to rate their pain : "Rate your pain from 0 (no pain) to 10 (unbearable pain)" 0 point is the minimum and 10 point is the maximum.
The higher the score, the more severe the pain.
|
40 minutes after transferred into the postanesthesia care unit
|
|
Pain measurement by the verbal rating scale
Time Frame: 5 minutes after transferred into the postanesthesia care unit
|
Patients verbally requested to answer which of the four categories you belong to : no pain, mild pain, moderate pain, severe pain
|
5 minutes after transferred into the postanesthesia care unit
|
|
Pain measurement by the verbal rating scale
Time Frame: 20 minutes after transferred into the postanesthesia care unit
|
Patients verbally requested to answer which of the four categories you belong to : no pain, mild pain, moderate pain, severe pain
|
20 minutes after transferred into the postanesthesia care unit
|
|
Pain measurement by the verbal rating scale
Time Frame: 40 minutes after transferred into the postanesthesia care unit
|
Patients verbally requested to answer which of the four categories you belong to : no pain, mild pain, moderate pain, severe pain
|
40 minutes after transferred into the postanesthesia care unit
|
|
nonresponse rate of the numerical rating scale
Time Frame: 1 year
|
the rate of assessment failures among the total number of assessment
|
1 year
|
|
nonresponse rate of the verbal rating scale
Time Frame: 1 year
|
the rate of assessment failures among the total number of assessment
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jin-Tae Kim, Ph.D., Seoul National University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 12, 2018
Primary Completion (Actual)
August 30, 2019
Study Completion (Actual)
August 30, 2019
Study Registration Dates
First Submitted
November 30, 2018
First Submitted That Met QC Criteria
December 5, 2018
First Posted (Actual)
December 7, 2018
Study Record Updates
Last Update Posted (Actual)
October 22, 2020
Last Update Submitted That Met QC Criteria
October 19, 2020
Last Verified
October 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SNUMR2-3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.