Last reviewed · How we verify
NCT00975845
BioCleanse Tibialis Tendon Anterior Cruciate Ligament (ACL) Study
trial testing BioCleanse Tibialis tendon in Anterior Cruciate Ligament Rupture in 40 participants. Completed in 9 November 2017.
9 November 2017
Quick facts
| Lead sponsor | RTI Surgical |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 40 |
| Start date | 9 November 2017 |
| Primary completion | 9 November 2017 |
| Estimated completion | 9 November 2017 |
| Sites | 1 location across United States |
Drugs / interventions tested
- BioCleanse Tibialis tendon
Conditions studied
- Anterior Cruciate Ligament Rupture — all drugs for Anterior Cruciate Ligament Rupture →
Sponsor
RTI Surgical
Who can join
Adults 18 to 60, any sex, with Anterior Cruciate Ligament Rupture. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
To compare the outcome of Anterior Cruciate Ligament (ACL) reconstruction performed using the tibialis allograft to historical outcomes of ACL reconstruction patients and to establish if any correlation exists between the age of the graft donor and the clinical outcomes.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
A Prospective, Double-Blind Evaluation of Anterior Cruciate Ligament Reconstruction With Tibialis Tendon Allograft: Donor Age Does Not Alter Outcomes.
Carter T, Norton A. · · 2023 · cited 1× · PMID 36866298 · DOI 10.1016/j.asmr.2022.11.025
Verify or expand the search:
- PubMed search for NCT00975845
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Anterior Cruciate Ligament Rupture
Currently open trials in the same condition.
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- NCT07333092 — Investigation of the Effects of Proprioceptive Exercises After Anterior Cruciate Ligament Surgery · NA · recruiting
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Other RTI Surgical trials
Trials by the same sponsor.
- NCT04171544 — Streamline Occipito-Cervico-Thoracic System Post-Market Clinical Follow-up · completed
- NCT03744013 — A Post Market Prospective Study of FORTIVA® 1mm Porcine Dermis · NA · completed
- NCT03699891 — Evaluation of the Fortilink IBF System With TETRAfuse Technology · completed
- NCT02587403 — A Comparison of Fortiva and Strattice Tissue Matrices in Complex, Ventral Hernia Repair · NA · 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 NCT00975845 (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 RTI Surgical
- Last refreshed: 1 November 2021
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/NCT00975845.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing