A prospective study on reliability and precision of Stryker ADAPT system

A prospective study on reliability and precision of Stryker ADAPT system - ADAPT

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000023457

Enrollment

120

Registered

2016-08-15

Start date

2016-08-02

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Proximal femoral fractures

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Patients who receive the procedure with gamma 3 locking nail system and Stryker ADAPT system due to femoral proximal fracture. 2) Patients aged 20 years and older. 3) Patients who agree on study specific Informed Consent Form 4) Patients are willing and able to comply with postoperative scheduled evaluations

Exclusion criteria

Exclusion criteria: 1) Female subjects who are pregnant. 2) Patients who diagnosed as systemic disease or metabolic disease. 3) Patients who are immunological disease or received excess steroid(>30days). 4) Patients who have active/latent infection. 5) Patients who are judged ineligible with reasonable reason by investigators.

Design outcomes

Primary

Measure	Time frame
Reliablity of Stryker ADAPT System	—

Countries

Japan

Contacts

Public ContactSatoru Motohashi

Stryker Japan K.K. Clinical Affairs

satoru.motohashi@stryker.com03-6894-8219

Outcome results