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Distal Radius Fractures in Adults: A Multi-Center Study in South Kivu

Epidemiological, Radiological, Therapeutic and Evolutionary Aspects of Distal Radius Fractures in Adults in South Kivu: a Multi-center Cross-sectional Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06901973
Enrollment
192
Registered
2025-03-30
Start date
2018-01-01
Completion date
2023-12-31
Last updated
2025-03-30

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

Conditions

Distal Radius Fracture

Keywords

DISTAL RADIUS FRACTURES

Brief summary

The goal of this observational study is to describe the epidemiological, radiological, therapeutic, and evolutionary characteristics of distal radius fractures in adults in the Bukavu Health District, South Kivu, DRC. . The main question it aims to answer is: • What are the epidemiological, radiological, therapeutic, and evolutionary characteristics of distal radius fractures in adults in South Kivu, and how does intrafocal nailing influence outcomes such as consolidation time and complication rates in this population? Participants who have already operated for distal radius fracture will be enrolled in this study.

Interventions

PROCEDUREIntrafocal pinning

Intrafocal pinning involves the percutaneous insertion of Kirschner wires to stabilize the distal radius fracture, often followed by plaster immobilization.

Sponsors

Official University of Bukavu
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
17 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 17 years or older at the time of injury. * Diagnosed with a distal radius fracture via clinical and radiological assessment. * Admitted, treated, and followed up at one of the 16 participating institutions. * Complete medical records available, including epidemiological, clinical, radiological, therapeutic, and outcome data.

Exclusion criteria

* Patients under 17 years of age. * Incomplete or missing medical records. * Fractures not involving the distal radius. * Patients transferred to non-participating facilities without follow-up data.

Design outcomes

Primary

MeasureTime frameDescription
Time to consolidation45 daysDefinition: The duration (in days) from the initiation of treatment with intrafocal pinning to radiological evidence of fracture healing (union), defined as the presence of bridging callus across the fracture site on X-ray. Measurement: Calculated retrospectively from medical records, reported as mean ± standard deviation (e.g., 47.56 ± 6.75 days in the study). Rationale: Consolidation time is a direct indicator of treatment success, reflecting the intervention's ability to stabilize the fracture and promote healing. It is critical in a resource-limited setting where prolonged recovery impacts patient function and healthcare burden. Data Source: Radiology reports and follow-up records.

Countries

Democratic Republic of the Congo

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026