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Efficacy of Extracorporeal Shockwave Therapy on Ultrasonographic Changes in de Quervain Tenosynovitis

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

De Quervain Disease

Treatments

Other: Traditional physical therapy program
Other: Extracorporeal Shockwave therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05782114
P.T.REC/012/004162

Details and patient eligibility

About

The current study will be conducted to explore the efficacy of ESWT on ultrasonographic changes, pain intensity level, upper limb function and hand grip strength in patients with de Quervain tenosynovitis.

Full description

De Quervain tenosynovitis (DQT) is a painful condition involving the tendons of the abductor pollicis longus (APL) and extensor pollicis brevis (EPB). The pathogenesis is generally defined as a stenosing condition of the first dorsal compartment of the wrist, characterized by thickening of the extensor retinaculum of APL and EPB, which can cause tendon gliding difficulties and impingement between the tendons and their fibrous sheaths.

The prevalence rate of DQT in the general population is 0.5% for males and 1.3% for females, with peak prevalence at the age of 40-60 years. Female prevalence is 6 to 10 times higher than that in men. De Quervain tenosynovitis is a repetitive strain injury consider postures where the thumb is held in abduction and extension to be predisposing factors. De Quervain tenosynovitis incidence increased by virtue of modern life conditions such as excessive computer use and increased use of cellular phones.

However, little research has been carried out to determine the therapeutic effects of ESWT in DQT, and up till now, there is a gap in literature that explore ESWT efficacy on ultrasonographic changes of DQT. So This current study will be conducted to explore the efficacy of ESWT on ultrasonographic changes, pain intensity level, upper limb function and hand grip strength in patients with de Quervain tenosynovitis.

Sixty patients from both genders will be involved in this study and will be randomly subdivided into two equal groups in number. First Group (A) (Experimental Group) will receive radial Extracorporeal Shockwave therapy plus Traditional physical therapy program and the second Group (B) (Control Group): This group will receive Traditional physical therapy program.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age from 18 to 65 years
  2. Both genders (males and females).
  3. Normal BMI ranges between 18.5:24.9 kg/m2.
  4. Patients will be referred from an orthopedist with diagnosis of DQT.
  5. Chronic pain more than 2 months.
  6. No history of undergoing physiotherapy modalities or corticosterone injection therapies for any reasons during the past month.
  7. De Quervain tenosynovitis patients will be diagnosed based on the standard criteria, including pain and tenderness in the lateral wrist and a positive result for the Finkelstein test.

Exclusion criteria

  1. History of undergoing physiotherapy modalities or corticosterone injection therapies for any reason during the past month.
  2. Subjects with other neurological disorders rheumatologic diseases causing wrist pain.
  3. Pregnancy.
  4. History of fracture or surgery on the hand.
  5. Severe trauma, and coagulation disorders.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

The experimental Group A
Experimental group
Description:
Extracorporeal Shockwave therapy (four sessions one session per week) +Traditional physical therapy program (Instruction to wear Thumb Spica splint, Ultrasound therapy, stretching exercise \& strengthening exercise) (two sessions per week for 4 weeks).
Treatment:
Other: Extracorporeal Shockwave therapy
Other: Traditional physical therapy program
The control Group B
Active Comparator group
Description:
Traditional physical therapy program (Instruction to wear Thumb Spica splint, Ultrasound therapy, stretching exercise \& strengthening exercise) (two sessions per week for 4 weeks).
Treatment:
Other: Traditional physical therapy program

Trial contacts and locations

1

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Central trial contact

Mostafa G Mahmoud, phd

Data sourced from clinicaltrials.gov

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