Last reviewed · How we verify
NCT02382341
BIOSURE™ HEALICOIL™ PK Bone In-growth Study
trial testing BIOSURE™ HEALICOIL™ PK Interference Screw in Deficiency of Anterior Cruciate Ligament in 12 participants. Completed in 4 January 2017.
4 January 2017
Quick facts
| Lead sponsor | Smith & Nephew, Inc. |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 12 |
| Start date | 12 September 2014 |
| Primary completion | 4 January 2017 |
| Estimated completion | 4 January 2017 |
Drugs / interventions tested
- BIOSURE™ HEALICOIL™ PK Interference Screw
Conditions studied
- Deficiency of Anterior Cruciate Ligament — all drugs for Deficiency of Anterior Cruciate Ligament →
Sponsor
Smith & Nephew, Inc. — full company profile →
Who can join
Adults 18 to 50, any sex, with Deficiency of Anterior Cruciate Ligament. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The study seeks to document the bone in-growth into the BIOSURE™ HEALICOIL PK screw as measured by CT scans. Patients' improvement in pain and function will also be followed through various outcome measures.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Bone ingrowth into open architecture PEEK interference screw after ACL reconstruction.
Lind M, Nielsen T, Sørensen OG, Mygind-Klavsen B, et al · · 2020 · cited 5× · PMID 32948982 · DOI 10.1186/s40634-020-00285-z
Verify or expand the search:
- PubMed search for NCT02382341
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Smith & Nephew, Inc. trials
Trials by the same sponsor.
- NCT07025304 — Post-Market Clinical Study to Evaluate the Safety and Effectiveness of REFLEX ULTRA 45 for Coblation Inferior Turbinate · NA · recruiting
- NCT06916728 — A Post Approval Multicenter 10 Year Follow-up Observational Trial of Marketed Product - MP01 vs. Surgical Standard of Ca · enrolling by invitation
- NCT06831448 — Human Participant Study of a Prototype Multilayer Foam Dressing on Intact Skin. · NA · completed
- NCT06700850 — Human Participant Study of Prototype Non-medicated Multilayer Foam Dressings on Intact Skin · NA · completed
- NCT06306716 — A Clinical Study on New Negative Pressure Wound Therapy Dressing in the Management of Chronic & Acute Wounds · terminated
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 NCT02382341 (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 Smith & Nephew, Inc.
- Last refreshed: 7 September 2020
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/NCT02382341.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing