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NCT03311633
Complications in Distal Radius Fracture
NA trial testing Percutaneous pinning time in Radius Fracture Distal in 60 participants. Completed in 23 April 2024.
20 April 2024
Quick facts
| Lead sponsor | Carlos A Acosta-Olivo |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 29 September 2017 |
| Primary completion | 20 April 2024 |
| Estimated completion | 23 April 2024 |
| Sites | 2 locations across Mexico |
Drugs / interventions tested
- Percutaneous pinning time
Conditions studied
- Radius Fracture Distal — all drugs for Radius Fracture Distal →
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):
-
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
Verify or expand the search:
- PubMed search for NCT03311633
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Carlos A Acosta-Olivo trials
Trials by the same sponsor.
- NCT04187014 — Oral Tranexamic Acid vs. Oral Aminocaproic Acid to Reduce Blood Loss After Total Hip Replacement · Phase 2 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03311633 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Carlos A Acosta-Olivo
- Last refreshed: 8 May 2024
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.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing