Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06616376
Status:
COMPLETED
Last Update Posted:
None
First Post:
2022-11-16
Brief Title:
The Affect Of An Anti-Embolism Stocking Protocol
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Affect Of An Anti-Embolism Stocking Protocol On The Development Of Early Venous Thromboembolia In Patients With Knee Artroplasty
Status:
COMPLETED
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study was conducted to determine the effect of anti-embolism stocking AES use protocol affected the development of early venous thromboembolism VTE in patients undergoing total knee arthroplasty TKA
The randomized controlled single-blind intervention study included 40 patients Experimental Group 20 Control Group 20 who underwent TKA surgery in a university hospitals Orthopedics and Traumatology clinic between 2019 and 2021 While the experimental group received the AES protocol one day before the operation and continued until the 10 th day after the operation the control group received AES on the 0 th day after the operation and remained in the patient until the 21st day after the operation In the study a Data Collection Form with DVT and PE signs and symptoms was used
The randomized controlled single-blind intervention study included 40 patients Experimental Group 20 Control Group 20 who underwent TKA surgery in a university hospitals Orthopedics and Traumatology clinic between 2019 and 2021 While the experimental group received the AES protocol one day before the operation and continued until the 10 th day after the operation the control group received AES on the 0 th day after the operation and remained in the patient until the 21st day after the operation In the study a Data Collection Form with DVT and PE signs and symptoms was used
Detailed Description:
The study was carried out at a university hospitals Orthopedics and Traumatology clinic Knee arthroplasty surgery is performed on an average of 85 patients per year in the hospital with a bed capacity of 1200 The Orthopedics and Traumatology clinic has 36 beds and 9 nurses on staff
In the clinic LMWH is given to patients who will have knee arthroplasty 12 hours before the procedure Following knee arthroplasty an elastic bandage is placed over the dressing on the operated extremity and AES is only applied to the intact extremity AES is dressed on both extremities after the elastic bandage is removed Foot movements begin on the first postoperative day and patients are mobilized on the first or second postoperative day Patients are admitted to the clinic for a period of 5-7 days LMWH application which began in the preoperative period continues in the postoperative period for approximately 21 days until the sutures are removed The AES usage protocol is not implemented in the clinic and no training is provided to patients regarding the use of AES by healthcare personnel After TKA surgery AES patients are dressed and it is recommended that they wear them without removing them for 21 days sutures are removed
In the clinic LMWH is given to patients who will have knee arthroplasty 12 hours before the procedure Following knee arthroplasty an elastic bandage is placed over the dressing on the operated extremity and AES is only applied to the intact extremity AES is dressed on both extremities after the elastic bandage is removed Foot movements begin on the first postoperative day and patients are mobilized on the first or second postoperative day Patients are admitted to the clinic for a period of 5-7 days LMWH application which began in the preoperative period continues in the postoperative period for approximately 21 days until the sutures are removed The AES usage protocol is not implemented in the clinic and no training is provided to patients regarding the use of AES by healthcare personnel After TKA surgery AES patients are dressed and it is recommended that they wear them without removing them for 21 days sutures are removed
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None