Evaluation of the Intraoperative Accuracy of 3D-planned and Guided Osteotomies of the Hand and Forearm (CARDFOREARM)
Primary Purpose
Posttraumatic or Congenital Bone Deformity
Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
EUDAMED CIV-14-03-011940
Sponsored by
About this trial
This is an interventional treatment trial for Posttraumatic or Congenital Bone Deformity
Eligibility Criteria
Inclusion criteria
- Posttraumatic or congenital bone deformity or pseudoarthrosis in the field of hand Surgery requiring correction by corrective osteotomy
- Clinical indication for a computer tomography scan of the forearms
- > 18 years old
- written informed consent
Exclusion criteria
- pregnant or nursing women
- other clinical significant accompanying symptoms (Tumor, infection)
- non-compliance of the patient to follow the clinical study protocol, drug or alcohol abuse
- Participation in a different clinical trial within the last 30 days before inclusion or during the study
Sites / Locations
- University Hospital Balgrist
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Interventional
Arm Description
3D-planned osteotomies with patient-specific guides
Outcomes
Primary Outcome Measures
3D difference between preoperative plan and surgery
For each reduced fragment the 3D difference in all 6 degrees of freedom (3xrotation, 3xtranslation) is quantified by comparing pre- and postoperative CT.
Secondary Outcome Measures
Surgical Outcome
The surgical outcome is assessed by comparing DASH- and PRWE-scores pre- and postoperatively.
Full Information
NCT ID
NCT02625038
First Posted
November 27, 2015
Last Updated
March 26, 2019
Sponsor
Balgrist University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02625038
Brief Title
Evaluation of the Intraoperative Accuracy of 3D-planned and Guided Osteotomies of the Hand and Forearm
Acronym
CARDFOREARM
Official Title
CT-based Evaluation of the Intraoperative Implementation Accuracy of 3D-planned Osteotomies of the Hand and Forearm Performed With Patient-specific Instruments
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
January 2019 (Actual)
Study Completion Date
January 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Balgrist University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Target of the study is to evaluate the reduction accuracy of 3D computer-planned osteotomies that are performed with patient-specific instruments.
Due to the higher accuracy achieved it is expected that complaints can be resolved or effectively revealed. The Research hypothesis to prove is "The medical product permits the surgical reduction of deformed bones of the hand and forearm (radius, ulna, distal humerus, carpal, metacarpal, and finger bones) by corrective osteotomy within an accuracy of 2 mm and 2º. Secondary outcome is an assessment of the surgical outcome using the "Disabilities of the Arm, Shoulder and Hand" (DASH) and the "Patient related wrist Evaluation" (PRWE) scores.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic or Congenital Bone Deformity
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
110 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Interventional
Arm Type
Experimental
Arm Description
3D-planned osteotomies with patient-specific guides
Intervention Type
Device
Intervention Name(s)
EUDAMED CIV-14-03-011940
Primary Outcome Measure Information:
Title
3D difference between preoperative plan and surgery
Description
For each reduced fragment the 3D difference in all 6 degrees of freedom (3xrotation, 3xtranslation) is quantified by comparing pre- and postoperative CT.
Time Frame
42 month
Secondary Outcome Measure Information:
Title
Surgical Outcome
Description
The surgical outcome is assessed by comparing DASH- and PRWE-scores pre- and postoperatively.
Time Frame
42 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria
Posttraumatic or congenital bone deformity or pseudoarthrosis in the field of hand Surgery requiring correction by corrective osteotomy
Clinical indication for a computer tomography scan of the forearms
> 18 years old
written informed consent
Exclusion criteria
pregnant or nursing women
other clinical significant accompanying symptoms (Tumor, infection)
non-compliance of the patient to follow the clinical study protocol, drug or alcohol abuse
Participation in a different clinical trial within the last 30 days before inclusion or during the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreas Schweizer, Prof.
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Balgrist
City
Zurich
ZIP/Postal Code
8008
Country
Switzerland
12. IPD Sharing Statement
Learn more about this trial
Evaluation of the Intraoperative Accuracy of 3D-planned and Guided Osteotomies of the Hand and Forearm
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