Comparison of Static and Dynamic Opening With Neural Sliding in Cervical Radiculopathy

Cervical Radiculopathy Clinical Trial

Official title:

Comparison of Static and Dynamic Opening With Neural Sliding in Cervical Radiculopathy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06154993
• Other study ID #: S22C08G30001
• Status: Recruiting
• Phase: N/A
• Start date: August 3, 2023
• Est. completion date: February 1, 2024

Study information

• Verified date: November 2023
• Source: Riphah International University
• Contact: Imran Amjad, Phd
• Phone: 03324390125
• Email: imran.amjad[@]riphah.edu.pk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this randomized controlled trial is to determine the effects of static and dynamic opening with neural sliding in patients with cervical radiculopathy for reducing pain, enhancing cervical range of motion and improve functional status.

Description:

Static opener is a neurodynamic technique for cervical radiculopathy for reducing pressure on the nervous system that causes intervertebral foramina to remain in the open position for a certain period. This enables blood flow to return to neural tissue so that oxygenation is improved, along with slider mobilization will reduce symptoms and give better healing to the inflamed nerve. when the intervertebral foramina remain open for a considerable amount of time axoplasmic flow is reestablished, oxygenation is improved, increases blood flow along with venous return and nerve gets more nutrients and all the inflammatory exudate is taken off resulting for early improvement. Dynamic opener is a neurodynamic technique in opening direction to repetitively open and close the intervertebral foramina and produces oscillatory movements that cause pumping effect on the nerve and help to drain edema due to inflammation and help reduce pain and increase the range also.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 36
• Est. completion date: February 1, 2024
• Est. primary completion date: December 1, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 35 Years to 60 Years

Eligibility

Inclusion Criteria:

• : • Spurling +ive
• Distraction test +ive (alleviate symptoms)
• Pain, paresthesia and numbness in Rt/Lt UL in dermatomal pattern of median nerve
• MRI confirmed spondylosis or disc herniation
• Age 35-60

Exclusion Criteria:

• • Cervical spine fracture
• RA
• Cervical myelopathy
• Systemic neurological conditions
• Osteoporosis

Related Conditions & MeSH terms

• Cervical
• Cervical Radiculopathy
• Radiculopathy

Intervention

Other:
• static opening with slider+ Conventional PT
Patient supine Maintaining neck flexion + contralateral flexion and rotation and applying median nerve slider mobilization while maintaining the neck static in mentioned position. Frequency: 3 sets of 10 reps with 5 sec hold for 3 times/week for 4 weeks Conventional PT includes hot pack for 10 mins and cervical isometrics. Frequency: 3 sets of 10 reps with 5 sec hold for 3 times/week for 4 weeks. Duration: 30-40 mins
• dynamic opener with slider + Conventional PT
Patient supine Neck flexion + contralateral flexion and rotation. And sliding the median nerve along with neck movement from contralateral flexion+rotation to neutal position in repetitive manner, by releasing tension from median nerve when bringing neck in neutral to ease tension from affected side. Conventional PT includes hot pack for 10 mins and cervical isometrics. Frequency: 3 sets of 10 reps with 5 sec hold for 3 times/week for 4 weeks. Duration: 30-40 mins

Locations

Country	Name	City	State
Pakistan	RehabWrox	Islamabad	Federal
Pakistan	Pakistan Railway General Hospital	Rawalpindi	Punjab

Sponsors (1)

Lead Sponsor	Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	neck disability index	Most used questionnaire for disability in patient related to any musculoskeletal neck condition. It has 7 items for daily living, 2 for pain and 1 for concentration. Each item is rated from 0 to 5. Total score is presented in percentage. Higher score tells greater disability while 0 means no disability. Total score is 50.	4 weeks
Primary	visual analogue scale	VAS is a commonly used assessment tool for pain intensity ranging from 0 to 100mm on a horizontal scale while patient marks a vertical line to rank his/her pain.; 0-4mm no pain 5-44mm mild pain 45-74mm moderate pain 75-100mm severe pain	4 weeks
Primary	inclinometer	A device used to check range of motion based on gravity.	4 weeks