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Clinical Trials/NCT07405008
NCT07405008Not yet recruitingNot Applicable

Effect of Laser Acupuncture on Carpal Tunnel Syndrome Post Aromatase Inhibitors in Breast Cancer Patient .

Cairo University1 site in 1 country54 target enrollmentStarted: March 1, 2026Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
54
Locations
1
Primary Endpoint
Median Motor Nerve Conduction Study

Study Overview

Brief Summary

The study will be carried out on a total number of fifty-four females with age ranged 40 - 60 years old suffering from CTS post mastectomy ,the patients will be randomly assigned into two groups equal in number (27 patients for each group from Damanhur Medical National institute).

  1. -Group (A): This group will include 27 patients will receive laser acupuncture technique 3 times per week in addition to traditional physical therapy program (myofascial release, nerve flossing ex., Tendon gliding ex. strengthening ex., ROM ex. and night splint) for 8 weeks.
  2. -Group (B): This group will include 27 patients will receive traditional physical therapy program (myofascial release, nerve flossing ex., Tendon gliding ex., strengthening ex., ROM ex. and night splint) for 8 weeks.

Detailed Description

The study will be carried out on a total number of fifty-four females with age ranged 40 - 60 years old suffering from CTS post mastectomy , the patients will be randomly assigned into two groups equal in number (27 patients for each group from Damanhur Medical National institute).

  1. -Group (A): This group will include 27 patients will receive laser acupuncture technique 3 times per week in addition to traditional physical therapy program (myofascial release, nerve flossing ex., Tendon gliding ex. strengthening ex., ROM ex. and night splint) for 8 weeks.
  2. -Group (B): This group will include 27 patients will receive traditional physical therapy program (myofascial release, nerve flossing ex., Tendon gliding ex., strengthening ex., ROM ex. and night splint) for 8 weeks.

Equipment:

  1. Measurement equipment:

  2. Nerve Conduction Studies (NCSs)

  3. Boston Carpal Tunnel Questionnaire (BCTQ)

  4. Hand-Held Dynamometer

  5. Therapeutic equipment:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
40 Years to 60 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • The subject selection will be according to the following criteria:
  • Patients' age will be ranged between 40-60 years old.
  • 54 Female patients had breast cancer will participate in this study.
  • All patients will have wrist pain and disability post AIS.
  • All patients will suffer from moderate to severe pain.
  • All patients will enroll to the study will have their informed consent

Exclusion Criteria

  • The potential participants will be excluded if they met one of the following criteria:
  • Patients with previous history of fracture at the wrist fracture.
  • History of any arthritis related to wrist.
  • Rheumatoid arthritis wrist secondary to fracture, dislocation,
  • Reflex sympathetic dystrophy and neurological disorder, Malignancy.
  • Epilepsy or any psychological disorders.

Arms & Interventions

LASER acupuncture technique plus traditional physical therapy

Experimental

Group A: 27 patients ,suffered from CTS post breast cancer treatment with Aromatase inhibitors, will receive Laser acupuncture technique in addition to traditional physical therapy program (myofascial release, nerve flossing ex., Tendon gliding ex. strengthening ex., ROM ex. and night splint)3 times per week for 8 weeks.

Intervention: LASER acupuncture technique (Device)

Traditional physical therapy program

Experimental

Group (B): 27 patients ,suffered from CTS post breast cancer treatment with Aromatase inhibitors , will receive traditional physical therapy program (myofascial release, nerve flossing ex., Tendon gliding ex., strengthening ex., ROM ex. and night splint) 3 times per week for 8 weeks.

Intervention: Traditional physical therapy (Other)

Outcomes

Primary Outcomes

Median Motor Nerve Conduction Study

Time Frame: 8weeks

With the help of electrode /conducting jelly, the recording was placed closed to motor of Abductor Policis Brevis and referance electrode 3 cm distal at the metacarpophalangeal joint. The ground electrode is placed between stimulation and recording electrode. A supramaximal stimulation was given at first to wrist and then at below. The difference between two latent period in msec gives the time taken by the impulses to travel from the elbow to the wrist.

Median Sensory Nerve Conduction Study:

Time Frame: 8 weeks

The Orthodromic conduction recording was done in this case. Here the recording electrode was placed 3cm proximal to the distal wrist crease 3cm proximal to the recording electrode. The ring electrode were placed in the second and third digit and it was used for stimulation of the nerve with the cathode placed at the proximal inter phalangeal. The grounding electrode was placed between stimulating electrode and grounding electrode.

Secondary Outcomes

  • Boston Carpal Tunnel Questionnaire (BCTQ)(8weeks)
  • Hand-Held Dynamometer (HHD)(8weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Naiera Sabry Mohamed Shams

Physiotherapy Specialist at Damanhur Medical National Institute, EL-Behira, Egypt

Cairo University

Study Sites (1)

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