Orthopedic Disorder Clinical Trial
Official title:
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™).
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™).
The purpose of this clinical investigation is to assess performance by collecting post-market performance and safety data. Outcome data collected from this pilot clinical investigation will provide descriptive data on performance and safety for Post-Market Surveillance (PMS) reporting, Clinical investigation Reports (CIR), and Clinical Evaluation Reports (CER). This France-based pilot clinical investigation will include 4 investigating sites. The sponsors are seeking to enroll 50 subjects undergoing surgery using HOLOBLUEPRINT™. The inclusion period is expected to take approximately 3 months, at an estimated rate of 13 subjects/month. In case of implant size difference or necessary changes between the preoperative planning and the actual device implanted, the patient will be excluded (Screen Failure) and no analysis will be performed. Each time an enrolled patient is operated using HOLOBLUEPRINT™, the site must enroll this patient consecutively, assuming the patient meets inclusion/non-inclusion criteria and provides their signed informed consent to participate (according to local requirements). This process of consecutive enrollment is one means of preventing patient selection bias and should strengthen the value of data collected in the pilot clinical investigation. Data will be collected preoperatively (baseline), during the surgical intervention, and in the immediate postoperative period (no later than 2 weeks postoperative). Then, a 6-month postoperative visit will complete the patient's participation in the pilot clinical investigation. At any time over the course of the clinical investigation, any adverse events will be recorded; both severity and a possible link to the clinical investigation device will be examined. The device included in the scope of this pilot clinical investigation is commercially available in Europe: Blueprint Mixed Reality HOLOBLUEPRINT™ used in combination with Blueprint Mixed Reality instruments. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05864833 -
METabolism After Orthopedic Surgery
|
||
| Completed |
NCT03286543 -
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System
|
N/A | |
| Recruiting |
NCT05461326 -
Quadriceps Tendon Versus Bone Patellar Tendon Bone Autograft ACL Reconstruction RCT
|
N/A | |
| Completed |
NCT06080685 -
Efficacy of Character Strengths Intervention in Enhancing Character Strengths and Self-esteem Among Adolescents
|
N/A | |
| Not yet recruiting |
NCT06326827 -
In'Oss™ (MBCP® Putty) Ortho
|
||
| Not yet recruiting |
NCT06002009 -
SupraScapular Cuff Study: Assessing the Effects of Size and Type of Rotator Cuff Tear on Suprascapular Nerve Function
|
||
| Completed |
NCT04730115 -
Evaluation of Architectural Changes in Mandibular Bone Pattern After Functional Treatment by Fractal Dimension Analysis
|
||
| Withdrawn |
NCT03436667 -
Perioperative Factors Impacting Surgical Risk and Outcomes in Children
|
||
| Completed |
NCT03299920 -
Opioid Consumption After Knee Arthroscopy
|
N/A | |
| Active, not recruiting |
NCT05075525 -
EFFECT OF HIGH INTENSITY LASER IN PATELLOFEMORAL PAIN SYNDROME
|
N/A | |
| Completed |
NCT06158165 -
Evaluating The Cardiovascular Effects of Tourniquet Application
|
||
| Recruiting |
NCT04891549 -
Tension Band Versus Locking Plate Fixation for the Treatment of Patella Fractures
|
N/A | |
| Recruiting |
NCT04676841 -
Wound Contamination During Orthopaedic Surgery
|
||
| Not yet recruiting |
NCT03899298 -
Safety and Clinical Outcomes With Amniotic and Umbilical Cord Tissue Therapy for Numerous Medical Conditions
|
Phase 1 | |
| Completed |
NCT04514601 -
A Quality Improvement Project to Assess and Refine the Handover Process at Morning Trauma Meetings
|
||
| Not yet recruiting |
NCT04546594 -
Epidemiological Data on Pain
|
||
| Completed |
NCT05396924 -
Rectal Temperature Measurement in Detecting Hypothermia During Hip Arthroscopy
|
N/A | |
| Active, not recruiting |
NCT06438835 -
Development & Evaluation of Pneumatic Artificial Muscle(PAM) for Patients With Ankle Foot Orthosis(AFO)
|
N/A | |
| Active, not recruiting |
NCT05795127 -
Risk for Reoperation After First MTP Joint Arthrodesis
|
||
| Completed |
NCT04481711 -
Total Knee Arthroplasty and Clinical Findings
|
N/A |