Last reviewed · How we verify
NCT06080412: BLUEMR
Blueprint® Mixed Reality Pilot Study
trial in Orthopedic Disorder in 44 participants. Completed in 7 May 2025.
14 August 2024
Quick facts
| Lead sponsor | Stryker Trauma and Extremities |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 44 |
| Start date | 8 February 2024 |
| Primary completion | 14 August 2024 |
| Estimated completion | 7 May 2025 |
| Sites | 4 locations across France |
Conditions studied
- Orthopedic Disorder — all drugs for Orthopedic Disorder →
- Arthritis Shoulder — all drugs for Arthritis Shoulder →
- Arthritis, Degenerative — all drugs for Arthritis, Degenerative →
- Cuff Tear Arthropathy — all drugs for Cuff Tear Arthropathy →
Sponsor
Stryker Trauma and Extremities — full company profile →
Who can join
18 and older, any sex, with Orthopedic Disorder or Arthritis Shoulder. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
A pilot Single-Arm, Multicenter, Prospective, Post-Market 6 months Follow-Up Clinical Investigation to Evaluate the Safety and Effectiveness of the Blueprint Mixed Reality HOLOBLUEPRINT™ (HOLOBLUEPRINT™).
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06080412
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Orthopedic Disorder
Currently open trials in the same condition.
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- NCT06869343 — Early Versus Delayed Rehabilitation After Reverse Total Shoulder Arthroplasty for Proximal Humerus Fracture · NA · recruiting
- NCT06877078 — Effect of Pre-Surgery Constipation Podcast: A RCT · NA · recruiting
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Other Stryker Trauma and Extremities trials
Trials by the same sponsor.
- NCT07118501 — A Prospective, Post-Market, Clinical Follow-up Study of the Incompass™ Total Ankle System · recruiting
- NCT06829667 — Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients Suffering From Lateral Ankle Instability · enrolling by invitation
- NCT05773352 — Perform® Humeral System - Fracture Study (PFX) · active not recruiting
- NCT06638138 — Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction of the Anterior Talofibular Ligament (ATFL · NA · enrolling by invitation
- NCT05523635 — Post Market Clinical Evaluation of Gamma 4 · active not recruiting
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 NCT06080412 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Stryker Trauma and Extremities
- Last refreshed: 16 September 2025
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/NCT06080412.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing