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Assessment and Rehabilitation in Cervical Radiculopathy
Sponsor: Filantropia Hospital
Summary
The investigators perform a prospective controlled study and analyse the effects of a rehabilitation program, including oral anti-inflammatory drugs, nutraceutical - ProHumano+ SpineDinamic (PHSD), physical therapy and kinetic measures on reduction of the severity of radicular pain, and improvement of the quality of life in participants with cervical radiculopathy (CR) over a relatively short period of treatment (three months). The major tasks in the assessment and management of CR are to exclude signs and/or symptoms of possible serious underlying pathology, to focus on an active approach to promote the natural recovery and to prevent chronicity through early tailored rehabilitation
Official title: Patient With Cervical Radiculopathy - Complete Assessment and Rehabilitation
Key Details
Gender
All
Age Range
50 Years - 79 Years
Study Type
INTERVENTIONAL
Enrollment
110
Start Date
2025-05-10
Completion Date
2025-08-15
Last Updated
2025-07-08
Healthy Volunteers
No
Conditions
Interventions
All patients in the study will be included in rehabilitation program
A total of 110 consecutive participants with previous diagnosed CR lasting more than 3 months will be enrolled in this study. After initial assessment, participants without surgical recommendation, will be included into two groups: Study Group will be received 10 sessions of rehabilitation program and nutraceutical product daily, 3 months, and Control Group will be received 10 sessions of rehabilitation program. The rehabilitation program include physical therapy (electrical muscle stimulation of the neck muscle and upper limb muscles , low-Level Laser Therapy and ultrasound) and kinetic training.
Study Group will receive a nutraceutical product daily, 3 months.
Study Group will receive a nutraceutical product daily, 3 months in addition to the rehabilitation program.
Locations (1)
Diana Kamal
Craiova, Romania