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The effect of Pregabalin on shoulder pain of patients with myofascial pain syndrome and central sensitization who undergo arthroscopic rotator cuff repair

Not Applicable
Conditions
Diseases of the musculoskeletal system and connective tissue
Registration Number
KCT0009403
Lead Sponsor
The Catholic University of Korea, Eunpyeong St. Mary's Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
76
Inclusion Criteria

?Patients aged 19 to under 70 who have been diagnosed with myofascial pain syndrome and are undergoing arthroscopic rotator cuff repair due to a tear of the rotator cuff.
?Patients with central sensitization (Central Sensitization Inventory (CSI) score of 40 or above).
?Patients who understand this study and consent to participate in it.

Exclusion Criteria

?Patients who are not central sensitization patients (Central Sensitization Inventory (CSI) score of 40 or below)
?Patients who have previously taken Pregabalin
?Patients who exhibit hypersensitivity reactions or severe complications after taking Pregabalin.
?Patients who have been diagnosed with and are being treated for psychiatric disorders
?Patients with localized infection, sepsis, or previous neurological abnormalities
?Patients with uncontrolled hypertension, evidenced by a resting blood pressure of more than 100 mmHg
?Patients with liver function abnormalities (aspartate aminotransferase or alanine aminotransferase >60 IU/litre).
?Patients with major cardiovascular diseases or renal impairments

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain VAS(Visual Analogue Scale)
Secondary Outcome Measures
NameTimeMethod
Funcional score
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