Overview

Clinical Study on the Effect of Tizanidine on the Function and Pain of Patients After Shoulder Arthroscopy

Status:
Not yet recruiting
Trial end date:
2027-06-01
Target enrollment:
0
Participant gender:
All
Summary
The perspective, randomized controlled trial is to investigate and evaluate the effect of Tizanidine on the function and pain of patients with rotator cuff tear after shoulder arthroscopy;
Phase:
Early Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Second Affiliated Hospital, School of Medicine, Zhejiang University
Treatments:
Buprenorphine
Celecoxib
Tizanidine
Criteria
Inclusion Criteria:

1 Patients who were diagnosed as supraspinatus tendon and infraspinatus tendon tear and
underwent shoulder arthroscopic surgery in the Second Affiliated Hospital of Zhejiang
University; 2 Age 20~70 years old; 3 Those with a long medical history, and symptoms such
as shoulder joint pain and weakness in a short period of time are obviously aggravated; 4.
After 3 months of medication and physical therapy, the symptoms and functions have not
improved significantly; 5 Volunteer to participate in this study, and the person and
his/her family members have given informed consent to the content of this study and signed
the consent form

Exclusion Criteria:

1. Patients with simple frozen shoulder;

2. Patients with shoulder joint tuberculosis, gout, tumor, rheumatoid disease or
infectious disease; 3. There are other joint pain factors before operation;

4 Patients with subscapularis tendon tear, long head tendinopathy requiring surgical
treatment, and severe shoulder synovitis were found during the operation; 5 Patients with
upper limb nerve injury, shoulder fracture, bone defect or severe osteoporosis; 6. Patients
with serious organ or hematopoietic system and other primary diseases; 7. Those who are
allergic to the drugs used in this study; 8 Women who are breast-feeding, pregnant or
preparing to become pregnant; 9 Patients with language and communication disorders, mental
history, cognitive dysfunction, etc. who cannot cooperate with the completion of nursing
intervention and research, and cannot complete the questionnaire required for this study.