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NCT06270173

Post-Market Study of The Tripod-Fix Vertebral Body Augmentation System in Osteoporotic Vertebral Compression Fractures

Active, enrolled NA Last updated 22 January 2025
What this trial tests

NA trial testing Tripod-Fix Vertebral Body Augmentation System (Tripod-Fix) in Osteoporotic Vertebral Compression Fractures in 53 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
16 February 2024
Primary endpoint
31 December 2025
28 February 2026

Quick facts

Lead sponsorWiltrom Co., Ltd.
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment53
Start date16 February 2024
Primary completion31 December 2025
Estimated completion28 February 2026
Sites4 locations across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Wiltrom Co., Ltd.

Who can join

18 and older, any sex, with Osteoporotic Vertebral Compression Fractures. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this Post-Market Clinical Follow-Up Study is to evaluate the safety and performance of the Tripod-Fix in the treatment of vertebral compression fractures (VCF) resulting from osteoporosis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Tripod-Fix Vertebral Body Augmentation System (Tripod-Fix)

Trials testing the same drug.

Other recruiting trials for Osteoporotic Vertebral Compression Fractures

Currently open trials in the same condition.

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/NCT06270173.

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