Pilot Study to Evaluate the Restore Orthobiologic Implant in Rotator Cuff Tear Repair

NCT ID: NCT00208338

Last Updated: 2016-07-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 33 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-07-31
• Study Completion Date: 2015-04-30

Brief Summary

Primary Endpoints:

Comparative evaluation of any differences between the two groups in change from baseline to the 3-month time point in terms of:

• Functional recovery (patient-based) - using the Oxford Shoulder Score.
• Functional recovery and early return of strength (pain, activities of daily living [ADL], range of motion [ROM], and power) - evaluated using the Constant Shoulder Assessment.
• Functional recovery (pain and function - patient-based), evaluated using the American Shoulder and Elbow Surgeons (ASES) Shoulder Assessment - patient self-report section.
• Region-specific Quality of Life - using the Western Ontario Rotator Cuff (WORC) Index.
• Range of motion - assessed by goniometer recorded as part of the Constant Score.
• Pain (taken from Pain visual analog scale [VAS] of the ASES Shoulder Assessment); and
• Record of escape pain medication usage (recorded in a daily patient diary).

Secondary Endpoints:

Comparative evaluation of any difference between the two groups in change from baseline to the 6-week time point, in terms of:

• Pain (taken from Pain VAS of the ASES Shoulder Assessment) and record of escape pain medication usage (recorded in a daily patient diary).

Comparative evaluation of any differences between the two groups in change from baseline to the 6-month time point, in terms of:

• Functional recovery (patient-based) - using the Oxford Shoulder Score.
• Functional recovery and early return of strength (pain, ADL, ROM, and power) - evaluated using the Constant Shoulder Assessment.
• Functional recovery (pain and function - patient-based), evaluated using the ASES Shoulder Assessment - patient self-report section.
• Region-specific Quality of Life - using the Western Ontario Rotator Cuff Index.
• Range of motion - assessed by goniometer recorded as part of the Constant Score.
• Pain (taken from Pain VAS of the ASES Shoulder Assessment) and record of escape pain medication usage (recorded in a patient diary).

Comparative evaluation of any difference between the two groups in change from baseline to the 6-week, 3, 6 and 12 month time points, in terms of health status - assessed by the EQ-5D instrument.

Conditions

Arm Injuries

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

1

Rotator cuff repair with RESTORE Porcine Small Intestine Submucosa patch (RESTORE SIS Patch) reinforcement

Group Type: EXPERIMENTAL

RESTORE SIS Patch

Intervention Type: DEVICE

Surgical repair of torn rotator cuff with RESTORE Porcine Small Intestine Submucosa patch (RESTORE SIS Patch) reinforcement

2

Standard rotator cuff repair

Group Type: ACTIVE_COMPARATOR

Rotator cuff repair

Intervention Type: PROCEDURE

Standard surgical repair of torn rotator cuff

Interventions

RESTORE SIS Patch

Surgical repair of torn rotator cuff with RESTORE Porcine Small Intestine Submucosa patch (RESTORE SIS Patch) reinforcement

Intervention Type: DEVICE

Rotator cuff repair

Standard surgical repair of torn rotator cuff

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Male or female subjects, aged 40 and above.
• Subjects who are able to give voluntary, written informed consent to participate in this investigation and from whom consent has been obtained.
• Subjects who, in the opinion of the Investigator, are able to understand this investigation, co-operate with the investigational procedures, and are willing to return to the hospital for all the required post-operative follow-ups.
• Subjects whose clinical symptoms and diagnosis suggest that they have a full-thickness rotator cuff tear (which includes but is not limited to the supraspinatus), which is degenerate in nature.

Exclusion Criteria

• Subjects who, in the opinion of the Investigator, have an existing condition that would prevent them from fulfilling the requirements of the Clinical Investigation Plan. (This should be detailed in the Screening Log.)
• Women who are pregnant.
• Subjects who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.
• Subjects who have participated in a clinical study with an investigational product in the last 6 months.
• Subjects who are currently known to be involved in any injury litigation claims relating to the shoulder being treated as part of the study.
• Subjects with a known allergy to porcine material or who, for religious or other reasons, are unwilling to accept a porcine-derived implant.
• Subjects who have undergone previous shoulder surgery (excluding purely-diagnostic arthroscopy).
• Subjects with significant paralysis of the shoulder.
• Subjects with inflammatory arthropathies.
• Subjects with active joint or systemic infection.

• Minimum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

DePuy International

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

U.Z. Gasthuis Berg

Leuven, , Belgium

Royal Liverpool University Hospital

Liverpool, , United Kingdom

Countries

Belgium; United Kingdom

Other Identifiers

CT 04/17

Identifier Type: -

Identifier Source: org_study_id