Ignite Creation Date:
2025-12-24 @ 5:30 PM
Ignite Modification Date:
2026-02-21 @ 11:35 PM
Study NCT ID:
NCT03084068
Status:
COMPLETED
Last Update Posted:
2019-12-18
First Post:
2017-03-14
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Use of Human Dehydrated Umbilical Cord Allograft in Supraspinatus Tendon Repair
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D000070599', 'term': 'Shoulder Injuries'}], 'ancestors': [{'id': 'D014947', 'term': 'Wounds and Injuries'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 25}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2017-02-01', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2019-12', 'completionDateStruct': {'date': '2019-01-17', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2019-12-17', 'studyFirstSubmitDate': '2017-03-14', 'studyFirstSubmitQcDate': '2017-03-14', 'lastUpdatePostDateStruct': {'date': '2019-12-18', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2017-03-20', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2019-01-17', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'ASES score', 'timeFrame': '12 months', 'description': 'The primary endpoint of the study is the number of subjects achieving a 20% increase from baseline in the overall ASES score at 12 months post-op.'}], 'secondaryOutcomes': [{'measure': 'Constant Murley Score', 'timeFrame': '12 months', 'description': 'Comparison of Constant scores between the two groups at each study time point'}, {'measure': 'Shoulder range of motion', 'timeFrame': '12 months', 'description': 'Assessment of the change in the range of motion of the shoulder joint for both treatment groups at each study time point.'}, {'measure': 'VAS Pain scores', 'timeFrame': '12 months', 'description': 'Change in patient reported pain from baseline'}, {'measure': 'Incidence of tendon re-tear', 'timeFrame': '12 months', 'description': 'Incidence of supraspinatus tendon re-tear in the two treatment groups as assessed by review of MRI scans by independent radiologists'}, {'measure': 'Incidence of adverse events', 'timeFrame': '12 months', 'description': 'Incidence of adverse events'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Shoulder Injury', 'Shoulder Sprain', 'Supraspinatus Tear']}, 'descriptionModule': {'briefSummary': 'To determine the effectiveness of human dehydrated umbilical cord allograft in standard open rotator cuff repair as assessed by the American Shoulder and Elbow Surgeons (ASES) score 12 months post-op.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n1. MRI confirmed diagnosis of a full thickness supraspinatus tendon tear necessitating surgical intervention (rotator cuff repair)\n2. Subject is male or female age 18 or older\n3. Subject is willing and able to provide informed consent and participate in all procedures and follow-up evaluations necessary to complete the study\n\nExclusion Criteria:\n\nSubjects who meet ANY of the following criteria will be excluded from the study:\n\n1. Shoulder pain primarily attributed to any of the following:\n\n 1. Ligament rupture due to use of fluoroquinolones\n 2. Capsular tear\n 3. Fracture of the humeral head\n 4. Inflammation of the joint or surrounding tissue (i.e. osteoarthritis, bursitis)\n 5. Neuropathic, radiating pain from conditions resulting in damage or inflammation of the nerve\n 6. Previous history of autoimmune connective tissue disorders (i.e. rheumatoid arthritis, systemic lupus erythematosus)\n2. Known history of poor compliance with medical treatments\n3. Subject has bilateral supraspinatus tendon tear\n4. Subject has signs and symptoms of an active infection of the shoulder joint\n5. Retraction of the supraspinatus tendon exceeding 1.5 cm in length\n6. Subject has additional injuries requiring further surgical intervention to the ipsilateral arm\n7. Subject has had previous surgery in the target arm within the past 6 months prior to treatment or plans to have surgery other than Rotator Cuff Repair in the target arm within 180 days of treatment\n8. Subjects currently receiving radiation therapy or chemotherapy\n9. Subjects has used an investigational drug, device or biologic within 12 weeks prior to treatment\n10. Subjects who are pregnant at enrollment or are planning to become pregnant within 180 days of treatment\n11. Subject has any significant medical condition(s) that, in the opinion of the Investigator, would interfere with protocol evaluation and participation\n12. Allergy or known sensitivity to aminoglycoside antibiotics such as gentamicin sulfate and/or streptomycin sulfate\n13. Workers' compensation patients"}, 'identificationModule': {'nctId': 'NCT03084068', 'briefTitle': 'Use of Human Dehydrated Umbilical Cord Allograft in Supraspinatus Tendon Repair', 'organization': {'class': 'INDUSTRY', 'fullName': 'MiMedx Group, Inc.'}, 'officialTitle': 'A Prospective, Randomized Controlled Trial for Rotator Cuff Repair - Efficacy of Supraspinatus Tendon Repair Using a Human Dehydrated Umbilical Cord Patch', 'orgStudyIdInfo': {'id': 'ACORT001'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Human umbilical cord allograft', 'description': 'Open Rotator Cuff Repair patched with human dehydrated umbilical cord allograft', 'interventionNames': ['Other: Human dehydrated umbilical cord allograft']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo Control', 'description': 'Open Rotator Cuff Repair with standard suture repair', 'interventionNames': ['Other: Placebo']}], 'interventions': [{'name': 'Human dehydrated umbilical cord allograft', 'type': 'OTHER', 'description': 'human dehydrated umbilical cord allograft', 'armGroupLabels': ['Human umbilical cord allograft']}, {'name': 'Placebo', 'type': 'OTHER', 'description': 'Open rotator cuff surgery with standard suture repair', 'armGroupLabels': ['Placebo Control']}]}, 'contactsLocationsModule': {'locations': [{'zip': '15090', 'city': 'Wexford', 'state': 'Pennsylvania', 'country': 'United States', 'facility': 'Hand & UpperEx Center', 'geoPoint': {'lat': 40.62646, 'lon': -80.05589}}], 'overallOfficials': [{'name': 'David Mason, MD', 'role': 'STUDY_DIRECTOR', 'affiliation': 'MiMedx Group, Inc.'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'MiMedx Group, Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}