NCT06210802

Brief Summary

This study aimed to validate Korean version of Defense and Veterans Pain Rating Scale for the assessment of postoperative pain.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 28, 2023

Completed
21 days until next milestone

First Posted

Study publicly available on registry

January 18, 2024

Completed
4 days until next milestone

Study Start

First participant enrolled

January 22, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 20, 2024

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 22, 2024

Completed
Last Updated

January 20, 2025

Status Verified

December 1, 2023

Enrollment Period

6 months

First QC Date

December 28, 2023

Last Update Submit

January 16, 2025

Conditions

Pain, Postoperative

Outcome Measures

Primary Outcomes (2)

  • Validity of K-DVPRS

    convergent validity and construct validity

    at postoperative 24 and 48 hours

  • Reliability of K-DVPRS

    test-retest reliability

    at postoperative 24 hours

Secondary Outcomes (1)

  • Evaluation success rate of K-DVPRS

    at postoperative 24 and 48 hours

Interventions

Korean version of Defense and Veterans Pain Rating ScaleOTHER

Defense and Veterans Pain Rating Scale translated into Korean

Eligibility Criteria

Age19 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients undergoing elective laparoscopic surgery or robot abdomen surgery (duration ≥ 1 hour) under general anesthesia in Seoul National University Hospital

You may qualify if:

  • Patients undergoing elective laparoscopic surgery or robot abdomen surgery (duration ≥ 1 hour) under general anesthesia

You may not qualify if:

  • Patients with ASA PS ≥ III
  • Patients with a difficulty to answer postoperative pain-related questions or K-DVPRS
  • Patients with red-green color blindness or difficulty distinguishing colors
  • Patients who are inappropriate for this clinical trial based on the investigator's opinionr

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Seoul National University Hospital

Seoul, Seoul, KS013, South Korea

Location

MeSH Terms

Conditions

Pain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 28, 2023

First Posted

January 18, 2024

Study Start

January 22, 2024

Primary Completion

July 20, 2024

Study Completion

October 22, 2024

Last Updated

January 20, 2025

Record last verified: 2023-12

Data Sharing

IPD Sharing
Will not share

Locations

KR(1)