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Clinical Trials/NCT06457529
NCT06457529Active, not recruitingNot Applicable

The Effect of Dry Needling and Prolotherapy on Pain, Function, and Quality of Life in Patients With Cervical Radiculopathy.

Superior University1 site in 1 country40 target enrollmentStarted: October 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
40
Locations
1
Primary Endpoint
Neck Disability Index

Study Overview

Brief Summary

Cervical radiculopathy is characterized by neurological dysfunction caused by compression and inflammation of the spinal nerves or nerve roots of the cervical spine. Rolotherapy is a regenerative therapeutic method that consists of injecting irritant solutions into the injured areas.

Detailed Description

Hyperosmolar dextrose is the most common agent. Administering proliferant substances can accelerate the tissue healing process by inducing cellular rupture and inflammatory response, leading to collagen deposition, cellular growth factor production, and regeneration. Dry needling used to relieve trigger point release in deep and superficial muscles. Both treatment interventions will apply to cervical radiculopathy patients to measure the effectiveness of treatment.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
20 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age group between 20-50 years
  • •Both male and female
  • •Unilateral pain starting in the cervical spine and radiating to the upper limb.
  • •Pain aggravated by upper limb movement
  • •Restricted range of motion of arm

Exclusion Criteria

  • •History of Spinal infection
  • •Spinal Cord Injury
  • •History of Vertebral tumor and factures
  • •History of cervical or intracranial surgery
  • •History of Radiating pain to bilateral upper limb.

Arms & Interventions

conventional treatment with Prolotherapy

Experimental

Intervention: conventional treatment with Prolotherapy (Diagnostic Test)

Dry Needling and conventional treatment

Other

Intervention: Dry Needling and conventional treatment (Other)

Outcomes

Primary Outcomes

Neck Disability Index

Time Frame: 12 Months

The NDI has become a standard instrument for measuring self-rated disability due to neck pain and is used by both clinicians and researchers. Each of the 10 items scores from 0 to 5. The maximum score is 50. The obtained score can be multiplied by two to produce a percentage score

WHO Quality of Life

Time Frame: 12 months

The QOLS is a reliable and valid instrument for measuring quality of life from the perspective of the patient. It focuses on domains that come from the qualitative descriptions of a wide range of adults across gender, cultural and language groups.Each individual item of the WHOQOL-BREF is scored from 1 to 5 on a response scale, which is stipulated as a five-point ordinal scale. The scores are then transformed linearly to a 0-100-scale (16, 17). The physical health domain includes items on mobility, daily activities, functional capacity, energy, pain, and sleep

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Naveed Babur

Principal Investigator

Superior University

Study Sites (1)

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