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Completed

NCT Number: NCT05423353

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yuzuncu Yil University

Van, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Paraffin Bath Therapy

Device

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

Extracorporeal Shock Wave Therapy

Device

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

Primary outcomes

  1. Visual Analogue Scale (VAS)

    Time frame: at baseline (before the treatment)

    patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse

  2. Visual Analogue Scale (VAS)

    Time frame: 2 weeks after baseline (at the end of treatment)

    patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse

  3. Visual Analogue Scale (VAS)

    Time frame: 6 weeks after baseline (one month after the end of treatment)

    patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse

  4. Duruöz Hand Index (DHI)

    Time frame: at baseline (before the treatment)

    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.

  5. Duruöz Hand Index (DHI)

    Time frame: 2 weeks after baseline (at the end of treatment)

    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. Duruöz Hand Index (DHI)

    Time frame: 6 weeks after baseline (one month after the end of treatment)

    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.

Sponsors and collaborators

Lead sponsor

Yuzuncu Yil University

Other

Registry information

Official study title

Comparative Effects of Paraffin Bath Therapy and Extracorporeal Shock Wave Therapy on Pain and Hand Functions in Patients With De Quervain Tenosynovitis

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jun 21, 2022
Registry last updated
Nov 29, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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