Outcome Analysis in fractures of the distal radius treated by OptivoHand vs. Cast

Outcome Analysis in fractures of the distal radius treated by OptivoHand vs. Cast - Optivo

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00012933

Enrollment

Registered

2017-08-24

Start date

2017-10-02

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

S52.5

Interventions

Group 1: Directly after reduction patients are receiving OptivoHand. This is to be used till treatment is finished. Group 2: Directly after reduction patients are receiving cast. This is to be used t

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: • distal Facture of the Radius AO 23 A2, A3, B1, B2, B3, C1, C2, C3 • Gustillo G0, G1 • Patients have to be able to participate

Exclusion criteria

Exclusion criteria: • Fix Ex • Non operative Treatment • Open fractures • forearme fractures • pathologic fractures • Patient not able to participate

Design outcomes

Primary

Measure	Time frame
Primary Aim of the study is the result of reduction by OptivoHand vs. Cast, checked directly after putting on Cast or OptivoHand by x-ray	—

Secondary

Measure	Time frame
secondary aims are patient satisfaction, DASH, SF-36. ROM (range of motion) by neutral Zero method and time off-work postoperativley. Patients are examend 2,4 amd 6 weeks as well as 6 and 12 months postoperativley.	—

Countries

Germany

Contacts

Public ContactAdrian Meder

Berufsgenossenschaftliche Unfallklinik Tübingen

ameder@bgu-tuebingen.de004970716063879

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026