Safety and Effect of Placentex Injection in Patient with Partial Tear of Rotator Cuff Tendon: An Open Label Study

Seoul National University Bundang Hospital0 个研究点目标入组 15 人开始时间: 待定最近更新: 2019年3月11日

试验速览

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•1)Who is not included in exclusion criteria of enrolling
•2)Who agree with a consent form after being explaned about the purpose and content of the treatment.
•3)Who is over 18 years old.
•4)Who has partial rotator cuff tear which is diagnosed with physical examination, simple x-ray, and sonographic test.
•5)The size partial rotator cuff tear is less than half of total depth, less than 1 cm in length.
•6)Do not respond to conservative management.
•7)Who does not have allergic reaction.
•8)Who does not suffer from psychologic disorder.

•1)Who disagree with this clinical test.
•2)Who has history of alcohol or opioid addiction.
•3)Who is having treatment of infectious disease.
•4)Who had a steroid or other injection management in 6 weeks.
•5)Who has arthritis, rheumatoid arthritis, synovitis, nerve entrapment, radiculopathy, septic arthritis, paralysis.
•6)Who has medical emergency, hemorrhagic disorder, contraindication to local injection.
•7)Who is pregnant or state of breast feeding.
•8)Who is malnutrient.
•9)Who has psychologic disorder.
•10)Who has hypotension of which blood pressure is less than 100 mmHg in systole and 60 mmHg in diastole.
•11)Who has liver or renal disease.
•12)Who is managed with vasoconstrictor.
•13)Who has severe medical disease such as diabetes or hepatitis.
•14)Who had medication for other clinical test in 3 months.
•15)Who is considered inappropriate other than above causes by test manager.
•16)Who has allergic reaction to this drug(PDRN).

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