ClinicalTrials.gg
Enrolling by invitationNCT07594639Updated Oct 30, 2026

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

An observational study in Osteoporosis, sponsored by AgNovos Healthcare, LLC. Enrolling by invitation at 1 site in Belgium. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by AgNovos Healthcare, LLC · Observational

Updated Oct 30, 2026Now Enrolling by invitationStart date moved+2 moreGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
305
Sex
All
01

Study summary

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.

02

Conditions studied

  • Osteoporosis

Keywords

  • Bone mineral density
  • Femoral strength
  • Hip fracture
  • Local osteo-enhancement procedure
  • LOEP
  • Proximal femur
  • Osteogenesis Imperfecta
  • OI
  • Hypophosphatasia
  • HPP
03

In context

Osteoporosis

1,601 studies on the registry are indexed under Osteoporosis; 209 are open to participants now.

This study's planned enrollment of 305 is above the median of 160 across 455 observational studies indexed under Osteoporosis.

Browse Osteoporosis studies →

Lead sponsor

AgNovos Healthcare, LLC is the lead sponsor of 10 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All subjects whose AGN1 LOEP treatment was performed outside of a prior AgNovos sponsored clinical study are considered for this study. The study anticipates enrolling up to 305 subjects. The final sample size may be smaller depending on willingness to participate or subject availability

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

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

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
305 participants (estimated)
Patient registry
No

Interventions

  • DeviceAGN1 LOEP

    Patients treated with AGN1 LOEP

06

What researchers measure

Primary outcomes

  1. Incidence of fragility fractures of AGN1 LOEP treated hip

    Time frame: Through study completion, an average of 6 months.

  2. Incidence of all adverse events and serious adverse events occurring intraoperative and post-AGN1 LOEP determined to be at least possibly related to the procedure and/or device

    Time frame: Through study completion, an average of 6 months.

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Not yet recruiting→Enrolling by invitation
changed Oct 30, 2026
Start date
Jun 1, 2026→Aug 25, 2026 (actual)
Oct 30, 2026
Primary completion
Sep 30, 2026→Apr 1, 2027
Oct 30, 2026
Study completion
Sep 30, 2026→Apr 1, 2027
Oct 30, 2026
Site contacts
Changed at 1 site. See the sites
Show the site
  • Vitaz · Sint-Niklaas, BelgiumContact removed j•••@vitaz.be
Oct 30, 2026
Show all 1 update
  1. Oct 30, 2026
    Not yet recruiting→Enrolling by invitation
    Start date Jun 1, 2026→Aug 25, 2026 (now actual)
    Primary completion Sep 30, 2026→Apr 1, 2027
    Study completion Sep 30, 2026→Apr 1, 2027
    Site contacts Changed at 1 site. See the sites
    Show the site
    • Vitaz · Sint-Niklaas, BelgiumContact removed j•••@vitaz.be
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07594639
Lead sponsor
AgNovos Healthcare, LLC
Responsible party
Sponsor
First posted
May 19, 2026
Start date
Aug 25, 2026
Primary completion
Apr 1, 2027 (estimated)
Completion
Apr 1, 2027 (estimated)
Last update
Oct 30, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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