Comparative Effects of Paraffin Bath Therapy and ESWT in Patients With De Quervain Tenosynovitis

NCT ID: NCT05423353

Last Updated: 2022-11-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-25

Study Completion Date

2022-10-19

Brief Summary

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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.

Detailed Description

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Conditions

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De Quervain Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Paraffin Bath Therapy

Paraffin bath therapy is a physical therapy method that can create a temperature increase of 7.5 °C in the joint capsule and 4.5 °C in the muscle.

Group Type ACTIVE_COMPARATOR

Paraffin Bath Therapy

Intervention Type DEVICE

Device named 'Fizyowax 1300' (Fizyomed, Turkey).

Extracorporeal Shock Wave Therapy

Extracorporeal shock wave therapy (ESWT) is a noninvasive treatment that involves delivery of shock waves to injured soft tissue to reduce pain and promote healing.

Group Type ACTIVE_COMPARATOR

Extracorporeal Shock Wave Therapy

Intervention Type DEVICE

Device named 'Elettronica Pagani,Italy' and will be used with radial probe.

Interventions

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Paraffin Bath Therapy

Device named 'Fizyowax 1300' (Fizyomed, Turkey).

Intervention Type DEVICE

Extracorporeal Shock Wave Therapy

Device named 'Elettronica Pagani,Italy' and will be used with radial probe.

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yuzuncu Yıl University

OTHER

Sponsor Role lead

Responsible Party

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Volkan Şah

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Volkan Şah

Role: PRINCIPAL_INVESTIGATOR

Yüzüncü Yıl Üniversitesi Tıp Fakültesi

Locations

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Yuzuncu Yil University

Van, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Van YYÜ School of Medicine

Identifier Type: -

Identifier Source: org_study_id

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