Polydeoxyribonucleotide (PDRN) for Cuff Regeneration
Primary Purpose
Rotator Cuff Tear
Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Polydeoxyribonucleotides
Normal saline
Sponsored by
About this trial
This is an interventional treatment trial for Rotator Cuff Tear focused on measuring healing, fatty degeneration, retear
Eligibility Criteria
Inclusion Criteria:
- definite rotator cuff tear on preoperative MRI, which needs repair
- acceptance of arthroscopic surgery including rotator cuff repair
Exclusion Criteria:
- history of ipsilateral shoulder operation or fracture
- concomitant neurological disorder around the
Sites / Locations
- Chuncheon Sacred Heart Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
PDRN(polydeoxyribonucleotide)
CONTROL(normal saline)
Arm Description
polydeoxyribonucleotide 3cc at surgery under arthroscopy guidance and 2 weeks after surgery under ultrasound guidance
normal saline 3cc at surgery under arthroscopy guidance and 2 weeks after surgery under ultrasound guidance
Outcomes
Primary Outcome Measures
American Shoulder and Elbow score
functional score of shoulder between 0 to 100(0: bad, 100: good)
Secondary Outcome Measures
Constant score
functional score of shoulder between 0 to 100(0: bad, 100: good)
Full Information
NCT ID
NCT03916198
First Posted
April 10, 2019
Last Updated
June 18, 2022
Sponsor
Chuncheon Sacred Heart Hospital
Collaborators
Ministry of Science and ICT
1. Study Identification
Unique Protocol Identification Number
NCT03916198
Brief Title
Polydeoxyribonucleotide (PDRN) for Cuff Regeneration
Official Title
Effect of Polydeoxyribonucleotide (PDRN) on Healing and Fatty Degeneration of Rotator Cuff in Human
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
May 9, 2019 (Actual)
Primary Completion Date
August 9, 2021 (Actual)
Study Completion Date
February 22, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chuncheon Sacred Heart Hospital
Collaborators
Ministry of Science and ICT
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is to evaluate the effect of polydeoxyribonucleotide (PDRN) for healing and fatty degeneration of rotator cuff. The investigators will enroll 130 patients with rotator cuff tear who will undergo arthroscopic rotator cuff repair. 130 patients will be classified into two group. One group (PDRN) will be injected at the repaired cuff with 3cc polydeoxyribonucleotide just after surgery and be injected with another 3ml polydeoxyribonucleotide under ultrasound guidance 2 weeks after the surgery. The other group (CONTROL) will be injected with 3ml normal saline in the same manner.
Detailed Description
Polydeoxyribonucleotide is a tissue regeneration activator. It binds an adenosine receptor and stimulate VEGF(vascular endothelial growth factor) synthesis and stimulate collagen synthesis. Nowadays, a lot of arthroscopic rotator cuff repairs are being performed. but the failure rate of rotator cuff repair is considerably high. Therefore, this study is to evaluate the effect of polydeoxyribonucleotide for healing and fatty degeneration of rotator cuff.
Visual analog scale (VAS) of pain and other functional scores of the two group will be checked preoperatively and postoperative 3, 6, 12, 24 months. Growth factors (VEGF, fibroblast growth factor(FGF), insulin like growth factor(IGF)) will be checked preoperatively and postoperative 1h, 2 days, 2 weeks, 6 weeks, 3, 6 months. Follow up MRI will be checked at postoperative 6 months. The parameters will be compared using statistical analysis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Tear
Keywords
healing, fatty degeneration, retear
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
79 participants with rotator cuff tear will be classified into two group. One group (PDRN) will be injected at the repaired cuff with 3cc polydeoxyribonucleotide just after surgery and be injected with another 3cc polydeoxyribonucleotide under ultrasound guidance 2 weeks after the surgery. The other group (CONTROL) will be injected with 3ml normal saline in the same manner.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
79 participants with rotator cuff tear will be randomly assigned to PDRN or CONTROL depending on the injection material. Randomization will be performed with a computerized random-sequence generator by an independent nurse.
Allocation
Randomized
Enrollment
79 (Actual)
8. Arms, Groups, and Interventions
Arm Title
PDRN(polydeoxyribonucleotide)
Arm Type
Experimental
Arm Description
polydeoxyribonucleotide 3cc at surgery under arthroscopy guidance and 2 weeks after surgery under ultrasound guidance
Arm Title
CONTROL(normal saline)
Arm Type
Placebo Comparator
Arm Description
normal saline 3cc at surgery under arthroscopy guidance and 2 weeks after surgery under ultrasound guidance
Intervention Type
Drug
Intervention Name(s)
Polydeoxyribonucleotides
Other Intervention Name(s)
PDRN
Intervention Description
Just after arthroscopic rotator cuff repair, 3cc polydeoxyribonucleotide will be injected, and 2 weeks after the surgery the same amount of the material will be injected.
Intervention Type
Drug
Intervention Name(s)
Normal saline
Intervention Description
Just after arthroscopic rotator cuff repair, 3cc normal saline will be injected, and 2 weeks after the surgery the same amount of the material will be injected.
Primary Outcome Measure Information:
Title
American Shoulder and Elbow score
Description
functional score of shoulder between 0 to 100(0: bad, 100: good)
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Constant score
Description
functional score of shoulder between 0 to 100(0: bad, 100: good)
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
definite rotator cuff tear on preoperative MRI, which needs repair
acceptance of arthroscopic surgery including rotator cuff repair
Exclusion Criteria:
history of ipsilateral shoulder operation or fracture
concomitant neurological disorder around the
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jung-Taek Hwang, MD,PhD
Organizational Affiliation
Chuncheon Sacred Heart Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chuncheon Sacred Heart Hospital
City
Chuncheon
State/Province
Gangwon-do
ZIP/Postal Code
24253
Country
Korea, Republic of
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
There is a privacy problem. The investigators should negotiate with our government about that.
Citations:
PubMed Identifier
20570301
Citation
Altavilla D, Squadrito F, Polito F, Irrera N, Calo M, Lo Cascio P, Galeano M, La Cava L, Minutoli L, Marini H, Bitto A. Activation of adenosine A2A receptors restores the altered cell-cycle machinery during impaired wound healing in genetically diabetic mice. Surgery. 2011 Feb;149(2):253-61. doi: 10.1016/j.surg.2010.04.024. Epub 2010 Jun 8.
Results Reference
background
PubMed Identifier
18318806
Citation
Galeano M, Bitto A, Altavilla D, Minutoli L, Polito F, Calo M, Lo Cascio P, Stagno d'Alcontres F, Squadrito F. Polydeoxyribonucleotide stimulates angiogenesis and wound healing in the genetically diabetic mouse. Wound Repair Regen. 2008 Mar-Apr;16(2):208-17. doi: 10.1111/j.1524-475X.2008.00361.x.
Results Reference
background
PubMed Identifier
29094396
Citation
Kang SH, Choi MS, Kim HK, Kim WS, Bae TH, Kim MK, Chang SH. Polydeoxyribonucleotide improves tendon healing following achilles tendon injury in rats. J Orthop Res. 2018 Jun;36(6):1767-1776. doi: 10.1002/jor.23796. Epub 2017 Nov 28.
Results Reference
result
Learn more about this trial
Polydeoxyribonucleotide (PDRN) for Cuff Regeneration
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