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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06241690
Other study ID # post-suture cold applications
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 11, 2021
Est. completion date July 20, 2022

Study information

Verified date January 2024
Source Firat University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose:This research was conducted as an experimental study with pretest and posttest control groups in order to evaluate the effect of post-suture cold applications on the pain level of children with sutures. Design and Methods: This study is a randomised controlled study. In the study, there were 150 children in the experimental group and 150 children in the control group.


Description:

The experimental groups was applied at the 1st, 2nd and 6th hours after the suture application in the cold applications The different practitioners applied in the Visual Analog Scale after and before in the cold applications to the experimental and control groups


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date July 20, 2022
Est. primary completion date December 15, 2021
Accepts healthy volunteers No
Gender All
Age group 12 Years to 17 Years
Eligibility Inclusion Criteria: - parents who agreed to participate in the study Exclusion Criteria: - -visually impaired child - mentally retarded child - speech impaired children - without chronic disease

Study Design


Related Conditions & MeSH terms


Intervention

Other:
the cold applications in post-suture pain reduces the child's pain
The experimental groups was applied cold applications immediately after 20 minutes the suture. Later, The experimental groups was applied cold applications again for 20 minutes 1 hour, 2 hours and 6 hours after the suture.

Locations

Country Name City State
Turkey Firat University Elazig Campus

Sponsors (1)

Lead Sponsor Collaborator
Firat University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary this study was measured the effects of cold application in the children after the suture The experimental groups was applied cold applications immediately after 20 minutes the suture. Later, The experimental groups was applied cold applications again for 20 minutes 1 hour, 2 hours and 6 hours after the suture. The visual Analog Scale were used as data collection tools. The Visual Analog Scale scale was applied before suturing. It was then applied 20 minutes, 1 hour, 2 hours and 6 hours after the suturing procedure.
The Visual Analog Scale: A minimum of 0 and a maximum of 10 points are obtained from the scale. A high score from the scale indicates a high level of pain
1 days
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