Ignite Creation Date:
2024-06-16 @ 11:50 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06445387
Status:
COMPLETED
Last Update Posted:
2024-06-06
First Post:
2024-05-16
Brief Title:
Pain During Femoral Sheath Removal in Patients Undergoing Percutaneous Coronary Intervenion
Sponsor:
Amasya University
Organization:
Amasya University
Study Overview
Official Title:
The Effect of Virtual Reality Glasses and Ice Applıcatıon on the Level of Pain During Femoral Sheath Removal in Patients Undergoing Percutaneous Coronary Intervenion
Status:
COMPLETED
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
It is to examine the effect of virtual reality and ice application on the pain level due to femoral sheath extraction
Detailed Description:
After obtaining the necessary permissions for the research the patients who were followed up in the hemodialysis unit of XY Z Hospitals were randomly divided into three groups virtual reality glasses application ice application and control group
Randomization Since the number of male and female patients was wanted to be kept equal simple randomization would not be possible so the stratified randomization method was used
Patients were assigned to groups in equal numbers according to their femoral sheath sizes In our clinic size 6 and 7 femoral sheaths are applied to male patients and number 6 femoral sheaths are applied to female patients Male patients were assigned to equal groups according to femoral sheath size 6 and 7
Since PCI is not performed in our clinic on weekends except for emergencies data were collected during working hours during a five-day weekday period
The pain level of the patients was evaluated using a numerical rating scale
before the femoral sheath extraction PAS1
during the femoral sheathing SDQ2
immediately after the femoral sheathing SDQ3
30 minutes after the femoral sheathing SDQ4 and
1 hour after the femoral sheathing SDQ4 SDÖ5 was evaluated and recorded
Randomization Since the number of male and female patients was wanted to be kept equal simple randomization would not be possible so the stratified randomization method was used
Patients were assigned to groups in equal numbers according to their femoral sheath sizes In our clinic size 6 and 7 femoral sheaths are applied to male patients and number 6 femoral sheaths are applied to female patients Male patients were assigned to equal groups according to femoral sheath size 6 and 7
Since PCI is not performed in our clinic on weekends except for emergencies data were collected during working hours during a five-day weekday period
The pain level of the patients was evaluated using a numerical rating scale
before the femoral sheath extraction PAS1
during the femoral sheathing SDQ2
immediately after the femoral sheathing SDQ3
30 minutes after the femoral sheathing SDQ4 and
1 hour after the femoral sheathing SDQ4 SDÖ5 was evaluated and recorded
Study Oversight
Has Oversight DMC:
None
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?:
None
Is an FDA AA801 Violation?:
None