Ignite Creation Date:
2024-07-17 @ 12:07 PM
Last Modification Date:
2024-10-26 @ 3:33 PM
Study NCT ID:
NCT06475963
Status:
RECRUITING
Last Update Posted:
2024-07-03
First Post:
2024-06-20
Brief Title:
Evaluation of Clinical Outcomes of Scaffold Treatment of Partial Meniscal Injuries of the Knee
Sponsor:
Istituto Ortopedico Rizzoli
Organization:
Istituto Ortopedico Rizzoli
Study Overview
Official Title:
Evaluation of Clinical Outcomes of Scaffold Treatment of Partial Meniscal Injuries of the Knee an Observational Study
Status:
RECRUITING
Status Verified Date:
2024-09
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:
STAR-ACT
Brief Summary:
The study consists of 3 phases Identification of includable patients Telephone follow-up evaluation and the collection of study-specific clinical data in medical records of enrolled patients
Identification by trained medical personnel of subjects who meet the studys inclusion criteria
Once the patients Informed Consent has been obtained the study-specific questionnaires will be submitted by telephone
Study-specific clinical score data will be collected from the medical records of patients enrolled in the study These data will be used together with the data collected during the telephone follow-up to evaluate the trend in outcomes over time after implantation of this scaffold
Identification by trained medical personnel of subjects who meet the studys inclusion criteria
Once the patients Informed Consent has been obtained the study-specific questionnaires will be submitted by telephone
Study-specific clinical score data will be collected from the medical records of patients enrolled in the study These data will be used together with the data collected during the telephone follow-up to evaluate the trend in outcomes over time after implantation of this scaffold
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