By InvitationNot Applicable

Assessment and Rehabilitation in Cervical Radiculopathy

Romania110 participantsStarted 2025-05-10

Plain-language 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

Who can participate

Age range50 Years – 79 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * patients older than 50 years of age; * lasting more than 3 months and diagnosed with CR confirmed by MRI in the last 6 months; * absence of other significant and disability upper limb osteoarthritis; * patients with stable cardiovascular and respiratory function, without unstable medical conditions; * compliance with physical exercise during the healthcare program. Exclusion Criteria: * pregnancy or breastfeeding; * need for surgical treatment; * intolerance to any component of the nutraceutical product; * malignancy; * modified laboratory test (ALT, AST, or Urea \>2x% reference range, Creatinine \>3x% reference range).

What they're measuring

Neck Disability Index

Timeframe: 3 months

Visual Analogue Scale For Pain

Timeframe: 3 months

Trial details

NCT IDNCT07054450

SponsorFilantropia Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-05-14

View on ClinicalTrials.gov More Cervical Radicular Pain trials