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NCT05559736

Artemis Proximal Femoral Nail for Internal Fixation of Intertrochanteric Femur Fractures

Withdrawn NA Last updated 31 December 2025
What this trial tests

NA trial testing Artemis Proximal Femoral Nail (PFN) implant in Intertrochanteric Fractures. Withdrawn.

Timeline
24 May 2023
Primary endpoint
31 December 2025
30 June 2026

Quick facts

Lead sponsorJohns Hopkins University
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date24 May 2023
Primary completion31 December 2025
Estimated completion30 June 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Johns Hopkins University

Who can join

18 and older, any sex, with Intertrochanteric Fractures or Femoral Fracture. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In February 2021, Altior Trauma Innovations™ announced that it had received 501(k) FDA approval for the Artemis Proximal Femoral Nail (PFN) System for internal fixation of intertrochanteric femur fractures. The objective of this pilot study is to evaluate safety, efficacy and feasibility of the Artemis PFN implant for operative fixation of intertrochanteric femoral fractures, compared to matched historical control patients who received other implants.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Intertrochanteric Fractures

Currently open trials in the same condition.

Other Johns Hopkins University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05559736.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing