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NCT07594639Enrolling by invitation

GRACE II (General Retrospective Analysis of Commercial Experience With AGN1 LOEP)

Retrospective Study of OSSURE LOEP in Osteopenic and Osteoporotic Subjects in the Commercial European Market

Source: ClinicalTrials.gov · Last updated 30 Oct 2026

Brief summary (registry, in English)

The study is designed as a retrospective, multicenter study for subjects previously treated with the AGN1 LOEP Kit in the proximal femur as part of standard hospital practice. This will be a non-randomized and non-blinded study. The study will collect retrospective data on the safety and performance of AGN1 LOEP of all subjects treated between September 2019 and January 2026. Subjects treated as part of an AgNovos prior protocoled study are excluded. Investigators are asked to reach out to all subjects that were previously treated with the AGN1 LOEP Kit in the proximal femur. Subject informed consent is obtained before a subject is enrolled into the study. Subjects treated but not enrolled are documented in a log with the reason why a subject did not participate. This log is kept on site. Enrolled subjects will be contacted per telephone to collect information about any fractures sustained post-AGN1 LOEP treatment.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
305 (estimated)
First submitted
6 May 2026
Start date
25 Aug 2026
Primary completion date
1 Apr 2027
Lead sponsor
AgNovos Healthcare, LLC
Diseases
Osteoporosis
NCT number
NCT07594639

What you commit to

  • Study type: Observational
  • Planned participants: 305
  • From 25 Aug 2026 to the primary completion date, 1 Apr 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • -The subject's AGN1 LOEP treatment was previously performed as part of an AgNovos prior protocoled clinical study.

Who the study is looking for

  • Subject has previously received AGN1 LOEP treatment in the proximal femur after September 2019 and before January 2026.
  • Subject can give written informed consent to allow for data collection. Obtaining informed consent is not required for deceased subjects.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Vitaz
Coordinator of this site? Confirm its status
Sint-NiklaasBelgiumUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.