Fiberfill - a new bone substitute for treatment of chronic osteomyelitis?

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00035647

Enrollment

Registered

2024-12-23

Start date

2024-11-14

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

chronic osteomyelitis M86.6

Interventions

Group 1: Bone reconstruction with Fiberfill of a patient with osteomyelitis

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Osteomyelitis (positiv bacteriology or histopathology)

Exclusion criteria

Exclusion criteria: non-compliance, e.g. regarding antibiotic therapie

Design outcomes

Primary

Measure	Time frame
Re-Infection at Follow-up after six months, clinical and radiographic control	—

Secondary

Measure	Time frame
Bone healing	—

Countries

Germany

Contacts

Public ContactHendrik Schöllmann

BG Klinikum Duisburg

hendrik.schoellmann@bg-klinikum-duisburg.de0049 203 7688 3620

Outcome results

None listed

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