Viewing Study NCT05046834


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Study NCT ID: NCT05046834
Status: WITHDRAWN
Last Update Posted: 2025-09-30
First Post: 2021-09-15
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Effect of Cold Application on Patient's Pain and Vital Signs During Chest Tube Removal.
Sponsor: Muğla Sıtkı Koçman University
Organization:

Study Overview

Official Title: Investigation of the Effect of Cold Application on Patient's Pain and Vital Signs During Chest Tube Removal.
Status: WITHDRAWN
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Researchers' workload and the fact that they work at different institutions made it difficult to gather data.
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: In this study, the effect of cold application used during and after chest tube removal on pain and vital signs in infants and children in the 0-3 age group will be examined.
Detailed Description: Purpose of the research:In this study, the effect of cold application used during and after breast tube removal on pain and life signs in infants and children aged 0-3 years will be examined.

Hypotheses:

H1: children who have cold application around the tube 15 minutes before chest tube removal have low pain scores during chest tube removal compared to other groups.

H2: Children whose skin temperature is lowered below 13.60 C before breast tube removal have lower pain scores compared to other groups.

H3: The cold application technique in the group of children affects the crying time after the procedure.

H4: The cold application technique in the group of children affects the signs of life before and after the procedure.

The research is a study in randomized controlled, prospective and cross-sectional design.

The data of the study will be collected using the Patient Identification Information Form, FLACC Pain Scale, Life Signs Follow-up Form.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: