Viewing Study NCT02019433


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Study NCT ID: NCT02019433
Status: TERMINATED
Last Update Posted: 2017-01-26
First Post: 2013-12-05
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Post Market Clinical Follow-Up of Acetabular Titan-Augment Structan®
Sponsor: Aesculap AG
Organization:

Study Overview

Official Title: Post Market Clinical Follow-Up of Acetabular Titan-Augment Structan®
Status: TERMINATED
Status Verified Date: 2017-01
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: Implant Survival as well as clinical and radiological Follow-Up of acetabular Titan-Augment Structan®
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: