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Inion OTPS Biodegradable Fixation System for the Ankle

NCT00300989 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 43

Last updated 2007-10-05

No results posted yet for this study

Summary

The purpose of the investigation is to compare post-operative fracture and wound healing using Inion OTPS Biodegradable Fixation System implants versus Conventional metal implants.

Conditions

  • Surgery

Interventions

DEVICE

Inion OTPS Biodegradable Fixation System

Sponsors & Collaborators

  • Inion Oy

    lead INDUSTRY

Principal Investigators

  • Ole Brink · Aarhus University Hospital

  • Terho Kainonen · Turku Universal Central Hospital

  • Geir Stray Andreassen · Ullevaal University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-12-31
Completion
2007-05-31

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00300989 on ClinicalTrials.gov