Ignite Creation Date:
2024-05-06 @ 3:52 PM
Last Modification Date:
2024-10-26 @ 1:58 PM
Study NCT ID:
NCT04786379
Status:
TERMINATED
Last Update Posted:
2023-12-08
First Post:
2021-02-24
Brief Title:
Surgical Management of Knee Septic Arthritis
Sponsor:
Texas Tech University Health Sciences Center El Paso
Organization:
Texas Tech University Health Sciences Center El Paso
Study Overview
Official Title:
Open vs Arthroscopic Treatment of Septic Arthritis in the Adult Native Knee A Prospective Trial
Status:
TERMINATED
Status Verified Date:
2023-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Due to lack of adequate patient sample size in a reasonable time period and lack of research support staff
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Surgical excisional debridement is the mainstay of management in septic arthritis with necessary decompression lavage debridement and partial synovectomy However there has been considerable debate over the optimal modality Most surgeons perform an open arthrotomy or arthroscopic debridement although serial aspiration can be considered as an option in very limited circumstances with patients who cannot tolerate surgery While open arthrotomy has been often utilized there has been an increasing number of proponents for arthroscopic treatment citing lower re-infection rates and better functional outcomes However there has been a lack of well-designed prospective studies comparing surgical treatment modalities for native knee septic arthritis The goals of this present study are to determine if arthroscopic management of septic arthritis in the native knee resulted in a lower number of surgeries and a shorter length of stay compared to open arthrotomy Secondary outcomes included differences in postoperative pain and improvements in Lysholm knee scores
Detailed Description:
None
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