← Back to Clinical Trials
Recruiting NCT07506200

NCT07506200 Neuromuscular Re-education on Pain, ROM and Disability in Cervical Radiculopathy

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07506200
Status Recruiting
Phase
Sponsor Riphah International University
Condition Cervical Radicular Pain
Study Type INTERVENTIONAL
Enrollment 52 participants
Start Date 2026-03-01
Primary Completion 2026-06-16

Eligibility & Interventions

Sex All sexes
Min Age 30 Years
Max Age 50 Years
Study Type INTERVENTIONAL
Interventions
Neuromuscular Re educationConventional Physical Therapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 52 participants in total. It began in 2026-03-01 with a primary completion date of 2026-06-16.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study explores the effectiveness of Neuromuscular Re-education compared to conventional therapies in managing pain, range of motion, and disability in patients with Cervical Radiculopathy

Eligibility Criteria

Inclusion Criteria: * Participants of Age between 30 and 50 years old. * Participants of both gender included. * Participants having Unilateral upper extremity pain, paresthesia, or numbness * Participants with Four positive findings required: * Positive Spurling's test * Positive distraction test * Positive upper limb tension test * Ipsilateral cervical rotation less than 60 degrees * Participants must have experienced pain for at least 3 months. * Participants must have a pain score of 4 to 6 on the 0-10 scale Exclusion Criteria: * Participants having prior cervical spine surgery. * Participants with Cervical vertebral fracture * Participants with severe osteoporosis, rheumatic disease, shoulder disease, or infection will be excluded. * Participants with vertebro-basilar artery insufficiency and diabetic neuropathy

Contact & Investigator

Central Contact

Munaab Khan, PhD

✉ muneeb.khan@riphah.edu.pk

📞 +923367993611

Principal Investigator

Javeria Ghazal, MS

PRINCIPAL INVESTIGATOR

Riphah International University

Frequently Asked Questions

Who can join the NCT07506200 clinical trial?

This trial is open to participants of all sexes, aged 30 Years or older, up to 50 Years, studying Cervical Radicular Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07506200 currently recruiting?

Yes, NCT07506200 is actively recruiting participants. Contact the research team at muneeb.khan@riphah.edu.pk for enrollment information.

Where is the NCT07506200 trial being conducted?

This trial is being conducted at Sialkot, Pakistan.

Who is sponsoring the NCT07506200 clinical trial?

NCT07506200 is sponsored by Riphah International University. The principal investigator is Javeria Ghazal, MS at Riphah International University. The trial plans to enroll 52 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology