Study for Microangulation and Clinical Evaluation and Safety of Microembolization after microembolization using angiography in patients with shoulder pain

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004720

Enrollment

Registered

2020-02-10

Start date

2020-02-24

Completion date

Unknown

Last updated

2020-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery : After sufficient explanation to the subjects with shoulder pain, the clinical evaluation and intervention will be carried out through the hospital for 5 days or less. Enforced Pre-

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Men and women over 19 years old 2) Patients with shoulder pain of more than 1 month due to shoulder pain (rotary cuff disease, adhesive arthritis, calcific tendinitis, etc.) 3) Those who have a cognitive function that can accurately express the pain area and extent 4) A person who fully understands the purpose and procedure of the research and wishes to participate in the clinical research through voluntary consent.

Exclusion criteria

Exclusion criteria: 1) Those who do not meet the age standard 2) Suspected cervical neuromyopathy on physical examination 3) Those who have had shoulder surgery within the last 6 months 4) Those who have received injection in the shoulder within the last month 5) A person who deems the researcher unsuitable for participation in clinical research due to other reasons

Design outcomes

Primary

Measure	Time frame
Current visual assess score(VAS-P1) accoring to movement current	—

Secondary

Measure	Time frame
visual assess score(VAS-P2, P3) of shoulder accoring to movement current;Shoulder Pain and Disability Index)	—

Countries

Korea, Republic of

Contacts

Public ContactSEUNGROK KANG

Chonbuk National University Hospital

Outcome results