Amniotic Membrane as an Adjunct Treatment for Hallux Rigidus
Primary Purpose
Hallux Rigidus
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Dorsal Cheilectomy without Amniotic Membrane Tissue Implantation
Dorsal Cheilectomy with Amniotic Membrane Tissue Implantation
Sponsored by
About this trial
This is an interventional treatment trial for Hallux Rigidus
Eligibility Criteria
Inclusion Criteria:
- Patients presented with an isolated diagnosis of type II hallux rigidus who are candidates for operative management with dorsal cheilectomy.
- Patients over the age of 18 able to consent to participate
- The subject is psychosocially, mentally, and physically able to understand and comply with the requirements of the study
Exclusion Criteria:
- < 18 years of age
- Patients that use ambulatory assistive devices
- Patients with systemic inflammtory arthritis
- Patient undergoing revision surgery for hallux rigidus to the ipsilateral extremity
- Patients with significant arthritis requiring alternative surgery other than dorsal cheilectomy
Sites / Locations
- OrthoCarolina
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Dorsal Cheilectomy no Amniotic Membrane Tissue Implantation
Dorsal Cheilectomy-Amniotic Membrane Tissue Implantation
Arm Description
Dorsal cheilectomy is a surgery for hallux rigidus(degenerative arthritis and stiffness due to bone spurs that affect the joint at the base of the big toe). No amniotic membrane will be used for this group.
Dorsal cheilectomy procedure with the addition of the amniotic membrane. Amniotic membrane represents a biologic therapy that has the ability to actively regulate myrofibroblast formation and activity within the joint space and surgical site
Outcomes
Primary Outcome Measures
American Orthopedic Foot and Ankle Society (AOFAS) score
Secondary Outcome Measures
Full Information
NCT ID
NCT01825356
First Posted
April 2, 2013
Last Updated
February 8, 2023
Sponsor
OrthoCarolina Research Institute, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT01825356
Brief Title
Amniotic Membrane as an Adjunct Treatment for Hallux Rigidus
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
April 8, 2013 (Actual)
Primary Completion Date
September 2019 (Actual)
Study Completion Date
November 10, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
OrthoCarolina Research Institute, Inc.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine whether patients undergoing a dorsal cheilectomy procedure with implementation of amniotic membrane tissue results in improved clinical and functional outcomes compared to a standard dorsal cheilectomy procedure.
Specific Aim 1:
To compare American Orthopedic Foot and Ankle Society (AOFAS) scores between patients undergoing dorsal cheilectomy to patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue.
Hypothesis 1: Clinical and functional outcomes, as measured by the AOFAS , in the patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue will be superior to those without.
Specific Aim 2:
To compare range of motion between patients undergoing dorsal cheilectomy to patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue.
Hypothesis 2: Patient to undergo dorsal cheilectomy and implantation of amniotic membrane tissue will demonstrate less postoperative stiffness as measured from the pre-and postoperative radiographs.
Specific Aim 3:
To compare Foot Function Index (FFI) scores between patients undergoing dorsal cheilectomy to patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue.
Hypothesis 3: Clinical and functional outcomes, as measured by the FFI, the patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue will be superior to those without.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hallux Rigidus
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Dorsal Cheilectomy no Amniotic Membrane Tissue Implantation
Arm Type
Active Comparator
Arm Description
Dorsal cheilectomy is a surgery for hallux rigidus(degenerative arthritis and stiffness due to bone spurs that affect the joint at the base of the big toe). No amniotic membrane will be used for this group.
Arm Title
Dorsal Cheilectomy-Amniotic Membrane Tissue Implantation
Arm Type
Experimental
Arm Description
Dorsal cheilectomy procedure with the addition of the amniotic membrane. Amniotic membrane represents a biologic therapy that has the ability to actively regulate myrofibroblast formation and activity within the joint space and surgical site
Intervention Type
Procedure
Intervention Name(s)
Dorsal Cheilectomy without Amniotic Membrane Tissue Implantation
Intervention Type
Procedure
Intervention Name(s)
Dorsal Cheilectomy with Amniotic Membrane Tissue Implantation
Primary Outcome Measure Information:
Title
American Orthopedic Foot and Ankle Society (AOFAS) score
Time Frame
6 Months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients presented with an isolated diagnosis of type II hallux rigidus who are candidates for operative management with dorsal cheilectomy.
Patients over the age of 18 able to consent to participate
The subject is psychosocially, mentally, and physically able to understand and comply with the requirements of the study
Exclusion Criteria:
< 18 years of age
Patients that use ambulatory assistive devices
Patients with systemic inflammtory arthritis
Patient undergoing revision surgery for hallux rigidus to the ipsilateral extremity
Patients with significant arthritis requiring alternative surgery other than dorsal cheilectomy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John K Ellington, MD
Organizational Affiliation
OrthoCarolina Research Institute, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
OrthoCarolina
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28207
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Amniotic Membrane as an Adjunct Treatment for Hallux Rigidus
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