Status:

UNKNOWN

Efficacy of Extracorporeal Shock Wave Therapy on Carpal Tunnel Syndrome Post Mastectomy Lymphedema

Lead Sponsor:

Cairo University

Conditions:

Carpal Tunnel Syndrome

Eligibility:

FEMALE

40-60 years

Phase:

NA

Brief Summary

Sixty eight female patients who had symptoms of carpal tunnel syndromesuch as wrist pain or numbness and paraesthesia and had lymphedema of an upper extremity.Their ages will be ranged from 40 to 60 y...

Detailed Description

In this study the patients will be randomly assigned into two equal groups(34 patients for each group)Group A (experimental group):This group includes 34female patients who will receive extra corporea...

Eligibility Criteria

Inclusion

  • All participants could be considered and enrolled if they conformed to the diagnosis of CTS, with clinical symptoms for at least 3 months.
  • The clinical symptoms and signs for the diagnosis of CTS were as follows:
  • Paresthesias and painful swelling with weakness of the affected hand, exacerbated while sleeping or by repetitive use of the wrist, which would be relieved by shaking the hand with postural change.
  • Sensory loss with numbness in the regions of the hand innervated by the median nerve;
  • Impaired motor function with atrophy of the median nerve-innervated thenar muscles.
  • Positive Tinel's sign.
  • The subject selection will be according to the following criteria:
  • Female patient their age range between 40-60 years.
  • Symptoms of CTS as pain, tingling sensation for at least 3 months.
  • Unilateral or bilateral Lymphedema following mastectomy
  • All patients enrolled to the study will have their informed consent.

Exclusion

  • The potential participants will be excluded if they meet one of the following criteria:
  • Local infections at the hand level.
  • Patients with prior medical histories of cardiac arrhythmias.
  • Patient with venous thrombosis.
  • Areas of skin with lesions and impaired sensation
  • Other diseases that cause significant swelling.
  • During pregnancy and breastfeeding.

Key Trial Info

Start Date :

November 1 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 1 2023

Estimated Enrollment :

68 Patients enrolled

Trial Details

Trial ID

NCT06131515

Start Date

November 1 2023

End Date

December 1 2023

Last Update

November 15 2023

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Khadra Mohamed Ali

Cairo, Egypt

2

Shahira Sami

Cairo, Egypt