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Clinical Trial Summary

The aim of the study is to compare the effectiveness of ultrasound-guided betamethasone and 5% dextrose injection, which is routinely applied in clinical practice, in patients with mild and moderate carpal tunnel syndrome (CTS).


Clinical Trial Description

It is planned as an observational, single-center clinical study.A total of 28 patients diagnosed with mild-moderate carpal tunnel syndrome who meet the inclusion criteria will be included in the study.Patients who had been experiencing trigger finger symptoms for at least three month and who presented to the Gaziler Physical Medicine and Rehabilitation Training and Research Hospital, affiliated with the Health Sciences University Faculty of Medicine. Patients will be divided into two groups. One group will receive 5% dextrose, the other group will receive 1 session of local injection by mixing Celeston chronodose [1ml/3 mg betamethasone acetate+3,947 mg betamethasone disodium phosphate (equivalent to 3 mg betamethasone)] and 1 ml 2% prilocaine. Evaluations will be made before injection, at weeks 4 and 12. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06360510
Study type Observational
Source Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Contact
Status Active, not recruiting
Phase
Start date May 5, 2023
Completion date May 5, 2024

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