De Quervain Disease Clinical Trial
Official title:
Comparative Effects of Paraffin Bath Therapy and Extracorporeal Shock Wave Therapy on Pain and Hand Functions in Patients With De Quervain Tenosynovitis
Verified date | November 2022 |
Source | Yuzuncu Yil University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
There is no study in the literature comparing both paraffin bath therapy and Extracorporeal Shock Wave Therapy (ESWT) in the treatment of patients with De Quervain Tenosynovitis. The aim of this study is performing this comparison.
Status | Completed |
Enrollment | 70 |
Est. completion date | October 19, 2022 |
Est. primary completion date | September 5, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Being 18 years or older - Meeting De Quervain diagnostic criteria - Not having applied any physical therapy modality to the hand-wrist in the last 1 month - Not using pain medication in the last 1 month, - Not using local anesthetics or steroid injections on the hand-wrist in the last 3 months - Have received written consent to participate in the study, and have come to the last control at the 6th week. Exclusion Criteria: - Neurological diseases (especially neuropathies), - Malignancy, - Rheumatological diseases - Pregnancy - History of hand/wrist fracture or surgery - Hand/wrist trauma in the last 1 month - Coagulation disorder diseases |
Country | Name | City | State |
---|---|---|---|
Turkey | Yuzuncu Yil University | Van |
Lead Sponsor | Collaborator |
---|---|
Yuzuncu Yil University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analogue Scale (VAS) | patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse | at baseline (before the treatment) | |
Primary | Visual Analogue Scale (VAS) | patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse | 2 weeks after baseline (at the end of treatment) | |
Primary | Visual Analogue Scale (VAS) | patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse | 6 weeks after baseline (one month after the end of treatment) | |
Primary | Duruöz Hand Index (DHI) | Duruöz Hand Index (DHI) is a functional disability scale that can be used successfully to assess the functional disability with different hand arthropathies. It consists of 18 items that evaluate hand and wrist activities. The answers are evaluated on a 6-level (0-5) Likert scale and the total score ranges from 0 to 90. | at baseline (before the treatment) | |
Primary | Duruöz Hand Index (DHI) | Duruöz Hand Index (DHI) is a functional disability scale that can be used successfully to assess the functional disability with different hand arthropathies. It consists of 18 items that evaluate hand and wrist activities. The answers are evaluated on a 6-level (0-5) Likert scale and the total score ranges from 0 to 90. | 2 weeks after baseline (at the end of treatment) | |
Primary | Duruöz Hand Index (DHI) | Duruöz Hand Index (DHI) is a functional disability scale that can be used successfully to assess the functional disability with different hand arthropathies. It consists of 18 items that evaluate hand and wrist activities. The answers are evaluated on a 6-level (0-5) Likert scale and the total score ranges from 0 to 90. | 6 weeks after baseline (one month after the end of treatment) |
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