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NCT03311633

Complications in Distal Radius Fracture

Completed NA Last updated 8 May 2024
What this trial tests

NA trial testing Percutaneous pinning time in Radius Fracture Distal in 60 participants. Completed in 23 April 2024.

Timeline
29 September 2017
Primary endpoint
20 April 2024
23 April 2024

Quick facts

Lead sponsorCarlos A Acosta-Olivo
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment60
Start date29 September 2017
Primary completion20 April 2024
Estimated completion23 April 2024
Sites2 locations across Mexico

Drugs / interventions tested

Conditions studied

Sponsor

Carlos A Acosta-Olivo — full company profile →

Who can join

Adults 18 to 90, any sex, with Radius Fracture Distal. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

BACKGROUND. Distal radius fractures (FRD) are up to 17% of all diagnosed fractures and are the most commonly treated fractures in adult orthopedic patients. The management could be either conservative or surgical, depending on AO bone fracture classification. The principles of good treatment involves an anatomical reduction with a proper immobilization that keep the reduction. OBJECTIVE. Determine if percutaneous pinning for six weeks versus three has major complications in distal radius fractures.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Percutaneous pinning for treating distal radial fractures in adults.
    Karantana A, Handoll HH, Sabouni A. · · 2020 · cited 16× · PMID 32032439 · DOI 10.1002/14651858.cd006080.pub3

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Trials by the same sponsor.

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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/NCT03311633.

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