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The Effect of Coolsense Method on Pain and Comfort in Hemodialysis Patients

NCT06144801 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2023-11-22

No results posted yet for this study

Summary

This study aimed to investigate the impact of the CoolSense method on arteriovenous fistula cannulation pain and the comfort levels of hemodialysis patients.

Conditions

  • Hemolysis
  • Complementary Therapy
  • Pain
  • Comfort

Interventions

DEVICE

CoolSense Group

Patients in the CoolSense group received a CoolSense device that had been pre-chilled in the freezer for a minimum of one hour. The cover of the CoolSense device was removed, and the arteriovenous fistula, whose metal tip had been cleaned with batikon, was brought into contact with the area where the arteriovenous fistula cannulation would occur. This contact was maintained for 5 seconds, involving circular movements, and the fistula cannulation took place promptly.

Sponsors & Collaborators

  • Gümüşhane Universıty

    collaborator OTHER

  • Karadeniz Technical University

    lead OTHER

Principal Investigators

  • Hatice Demirağ, Assist Prof. · Gümüşhane Universıty

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-20
Primary Completion
2023-07-31
Completion
2023-08-20

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06144801 on ClinicalTrials.gov