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Low Level Laser Versus Neural Mobilization of Brachial Plexus on Shoulder Dysfunction Post Liver Donation

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

Shoulder Pain

Treatments

Other: Neural mobilization techniques
Other: Conventional physical therapy program
Other: Low level laser therapy (LLLT)

Study type

Interventional

Funder types

Other

Identifiers

NCT06703775
P.T.REC/012/005253

Details and patient eligibility

About

The purpose of the study will be to compare therapeutic effect of low level laser versus neural mobilization techniques on shoulder dysfunction post liver donation.

Full description

The need for this study develops from the lack of information in the published studies about the effectiveness of low level laser and neural mobilization of brachial plexus on shoulder dysfunction post liver donation.

Following liver donation and transplantation, shoulder dysfunction and discomfort occur in 20% to 60% of patients.

Low-level laser therapy (LLLT) has been used as a non-pharmacological alternative to treat painful musculoskeletal conditions. It is used in acute, chronic painful and inflammatory affections shows that low energy irradiation from lasers alters cellular processes, producing anti-inflammatory effects and increased collagen turnover.

Neural mobilization (NM) is an intervention aimed at restoring the homeostasis in and around the nervous system, by mobilization of the nervous system itself or the structures that surround the nervous system. Neural mobilization facilitates movement between neural structures and their surroundings (interface) through manual techniques or exercise. Human and animal studies revealed that NM reduces intraneural edema, improves intraneural fluid dispersion, reduces thermal and mechanical hyperalgesia and reverses the increased immune responses.

The present study is designed to investigate the effect of LLLT versus NMT on shoulder dysfunction post liver donation.

Enrollment

66 estimated patients

Sex

All

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients are both males and females.
  • Their age will range from (20-50) years.
  • Patients will suffer from unilateral shoulder pain(Rt shoulder).
  • Patients will begin the training program one week post.operative.
  • All patients will suffer from moderate to severe pain (VAS score > 4).
  • Patients will be given their informed consent.

Exclusion criteria

  • Known history of high level Spinal cord injury and malignancy
  • Metabolic disease with a neurological component such as diabetes.
  • Orthopedic disorders such as fracture or dislocation.
  • Musculoskeletal disorders that will impair performance during training and tests.
  • Uncontrolled cardiovascular or pulmonary diseases .
  • Circulatory disturbances of upper extremity
  • Psychiatric illness, severe behavior or cognitive disorders.
  • Uncooperative patients.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

66 participants in 3 patient groups

Low level laser therapy (LLLT) + Conventional physical therapy program
Experimental group
Description:
This group will be composed of 22 patients with shoulder dysfunction post liver donation. Patients will receive low level laser in addition to conventional physical therapy program. LLLT will be applied for 3 times a week for 4 consecutive weeks.
Treatment:
Other: Low level laser therapy (LLLT)
Other: Conventional physical therapy program
Neural mobilization techniques + Conventional physical therapy program
Experimental group
Description:
This group will be composed of 22 patients with shoulder dysfunction post liver donation. Patients will receive neural mobilization techniques in addition to conventional physical therapy program. Exercises will be applied for 3 times a week for 4 consecutive weeks.
Treatment:
Other: Conventional physical therapy program
Other: Neural mobilization techniques
Conventional physical therapy program
Active Comparator group
Description:
This group will be composed of 22 patients with shoulder dysfunction post liver donation. Patients will receive conventional physical therapy program. Exercises will be applied for 3 times a week for 4 consecutive weeks.
Treatment:
Other: Conventional physical therapy program

Trial contacts and locations

1

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Central trial contact

Hayam Abd Elrazek Mohamed, M.Sc; Hussein Gamal Hussein Mogahed, PhD

Data sourced from clinicaltrials.gov

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