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Development and Validation of a Calibrated Pneumatic Cervical Traction Device and Assessment of Its Effects on Selected Clinical Variables of Cervicobrachial Radiculopathy

Development and Validation of a Calibrated Pneumatic Cervical Traction Device and Assessment of Its Effects on Selected Clinical Variables of Cervicobrachial Radiculopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202507871039566
Enrollment
64
Registered
2025-07-08
Start date
2019-11-15
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Diseases Nervous System Diseases

Interventions

NCPCTD Group
CPCTD Group
OTDCTD Group

Sponsors

Anikwe Ernest Emezie
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants in this study were individuals; 1. Who presented with neck pain and associated radicular symptoms to the upper limb(s). 2. Who met the following criteria for diagnosing cervico-brachial radiculopathy (Wainner et al, 2003); a) Positive Spurling’s sign. b) Positive upper limb tension tests. c) Positive cervical spine compression and distraction test. d) Cervical spine rotation less than 60° towards the side of the target upper limb.

Exclusion criteria

Exclusion criteria: Individuals with cervicobrachial radiculopathy were excluded from this study if they; 1. Suffered from cervico-brachial radiculopathy along with any of the following; vascular disorders, diabetic neuropathy and radiculopathy due to tumour. 2. Had cervical spine pathology such as fracture, spondylolisthesis of greater than or equal to 50% and acute ligamentous injury. 3. Had a clinical condition that contradicts the use of traction and other physiotherapy treatment regimens such as; osteoporosis of the cervical spine etc (Furlan and Duso, 2018). 4. Had psychological or psychosomatic disorders, infections of the spine, known congenital abnormality of the nervous system and serious comorbidities or indications for immediate surgical intervention.

Design outcomes

Primary

MeasureTime frame
Pain;Range of Motion

Secondary

MeasureTime frame
Level of Disability

Countries

Nigeria

Contacts

Public ContactErnest Anikwe

Premier Physiotherapy and Rehabilitation Clinic

eeanikwe@gmail.com+2348034554600

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026