The Effect of Microfracture Procedure on Rotator Cuff Tendon Healing

Sponsor
Göker Utku değer (Other)
Overall Status
Suspended
CT.gov ID
NCT04421417
Collaborator
(none)
30
1
2
24
1.3

Study Details

Study Description

Brief Summary

Patients with complaints of shoulder pain or limitation of motion and had rotator cuff rupture diagnosed with magnetic resonance imaging will be analyzed and the patients with surgical indication will be included in a randomized fashion. One group of patient will undergo standard arthroscopic rotator cuff repair, while the other group will have microfracture procedure in addition to the standard arthroscopic repair. Before the operation, functional and clinical conditions will be recorded with Constant and American Shoulder and Elbow Surgeons Shoulder Score (ASES) universal shoulder scoring systems and Visual Analogue Scale(VAS) pain scale. The blood supply and healing of the tendon in the repair area will be compared by the doppler ultrasound (superb microvascular imaging) at the 2nd, 4th, 8th and 12th week after the operation. Post-operative clinical, functional status and pain levels will be evaluated with Constant, ASES and VAS pain scales at 24th week.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Microfracture + Standard Arthroscopic Rotator Cuff Repair
  • Procedure: Standard Arthroscopic Rotator Cuff Repair
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Treatment
Official Title:
Early-term Effects of Microfracture on Tendon Vascularity and Healing in Arthroscopic Treatment of Chronic Rotator Cuff Tears: A Prospective Randomized Trial
Actual Study Start Date :
Sep 15, 2020
Actual Primary Completion Date :
Sep 15, 2021
Anticipated Study Completion Date :
Sep 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Standard Arthroscopic Rotator Cuff Repair

Procedure: Standard Arthroscopic Rotator Cuff Repair
Standard Arthroscopic Rotator Cuff Repair

Experimental: Microfracture and Arthroscopic Rotator Cuff Repair

Procedure: Microfracture + Standard Arthroscopic Rotator Cuff Repair
drilling of rotator cuff footprint area on humerus and standard arthroscopic rotator cuff repair

Outcome Measures

Primary Outcome Measures

  1. assessing early change of tendon and footprint area vascularity [4th week]

    we will evaluate it by superb microvascular imaging via ultrasound, this ultrasound software give us quantitative value of vascularity

  2. assessing early change of tendon and footprint area vascularity [8th week]

    we will evaluate it by superb microvascular imaging via ultrasound, this ultrasound software give us quantitative value of vascularity

  3. assessing early change of tendon and footprint area vascularity [12th week]

    we will evaluate it by superb microvascular imaging via ultrasound, this ultrasound software give us quantitative value of vascularity

Secondary Outcome Measures

  1. functional outcome [24th week]

    This entity will be asses by functional scoring systems.These are American Shoulder and Elbow Surgeons Shoulder Score (ASES) and Constant Shoulder Score. The ASES is a composite instrument, requiring both a physician assessment and a patient-completed portion; however, it is commonly presented as solely the patient-reported survey. This includes a section on pain (7 items) and a section on activities of daily living (10 items). Scores range from 0 to 100 with a score of 0 indicating a worse shoulder condition and 100 indicating a better shoulder condition. Constant Score was designed to assess the functional state of a normal, a diseased, or a treated shoulder.The Constant score contains both physician-completed and patient-reported portions. The four domains include pain (15 possible points), activities of daily living (20 possible points), mobility (40 possible points), and strength (25 possible points). Scores range from 0 points (most disability) to 100 points (least disability).

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • degenerative rotator cuff tears
Exclusion Criteria:
  • traumatic rotator cuff tears

  • rheumatoid diseases

  • previous surgery of rotator cuff tendon

  • glenohumeral arthritis

  • acromioclavicular arthritis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istanbul University- Cerrahpasa Cerrahpasa Medical Faculty Istanbul Turkey 34098

Sponsors and Collaborators

  • Göker Utku değer

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Göker Utku değer, Research assistant, Istanbul University-Cerrahpasa
ClinicalTrials.gov Identifier:
NCT04421417
Other Study ID Numbers:
  • 2019-78167
First Posted:
Jun 9, 2020
Last Update Posted:
Nov 19, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Göker Utku değer, Research assistant, Istanbul University-Cerrahpasa
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 19, 2021