Clinical Trials Logo

Clinical Trial Summary

Cervicogenic angina (CA) is defined as paroxysmal angina- like pain that originates from the disorders of the cervical spine or other neck structures. Because CA mimics typical cardiac angina, symptoms in the elderly with cervical spondylosis are more frequently misdiagnosed Nakajima H, 2006. Patients with CA may have suffered symptoms for longer periods of time and seen several clinicians due to conflicting cardiac exams. Clinicians and patients are unaware that CA symptoms are stemming from cervical spine disorders. However, the mechanism of pain occurrence in patients with CA remains unclear.


Clinical Trial Description

Randomized Control Trail (RCT) will be used in the study. Participants will be divided into two groups (experimental and control groups). Each group will include 30 participants. The study population will be employees working in JU from different departments. A total of 60 participants will be included in the study. Their weight ranged from (50 kilograms) to (100 kilograms). And their height ranged from (150 centimeters) to (190 centimeters). And their body mass index ranged from (22.2) to (27.7). This will be divided into 2 groups with 30 participants in each group. The data collected will focus on measuring the Range of Motion (ROM) of the cervical spine using an Electro-Goniometer, the pain using Visual Analogue Scale (VAS), and the Hart Rate (HR) using an electro cardio Graphic (ECG). The study setting will be JU, located in Jerash City, Jordan. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06309849
Study type Interventional
Source South Valley University
Contact
Status Not yet recruiting
Phase N/A
Start date April 20, 2024
Completion date June 1, 2024

See also
  Status Clinical Trial Phase
Recruiting NCT06102304 - Myo-Electrical and Nerve Root Function Response to Focused Extracorpeal Shock Wave in Cervical Radiculopathy N/A
Recruiting NCT06220799 - Impact of Craniovertebral Angle on Dizziness and Risk of Falling in Cervical Radiculopathy Patients
Completed NCT01944150 - Association of Transcutaneous Electrical Nerve Stimulation and Hypnosis N/A
Recruiting NCT01495728 - Thoracic Manipulation in Patients With Cervical Radiculopathy N/A
Active, not recruiting NCT00695006 - Manual Therapy, Exercise and Traction for Patients With Cervical Radiculopathy: A RCT N/A
Completed NCT00344890 - Safety Study of Preservon-Treated Bone Implants for Cervical Fusion in the Treatment of Cervical Radiculopathy or Myelopathy N/A
Completed NCT03382821 - Comparative Trial Via Tranforaminal Approach Versus Epidural Catheter Via Interlaminar Approach Phase 4
Completed NCT04915222 - Manual Cervical Traction and Natural Apophyseal Glides for Cervical Radiculopathy Patients N/A
Recruiting NCT06043934 - Neural Mobilization With Intermittent Cervical Traction on Grip Strength, Sleep Quality, and Quality of Life in Cervical Radiculopathy N/A
Recruiting NCT06040047 - Prediction of Cervical Radiculopathy Success With PNF and Mobilization N/A
Completed NCT04544683 - Effectiveness of Cervical Transforaminal Epidural Steroid Injection Phase 4
Active, not recruiting NCT03674619 - Cervical Radiculopathy Trial N/A
Completed NCT04597112 - Effect of Myofascial Release Technique In Patients With Unilateral Cervical Radiculopathy N/A
Completed NCT04598113 - Effect of Cervical Traction on Balance in Cervical Radiculopathy Patients N/A
Recruiting NCT06339970 - Effects of Slider Versus Tensioners Nerve Gliding in Cervical Radiculopathy. N/A
Withdrawn NCT02694250 - Evaluation of Cervical Fusion With DTRAX® Cervical Cage With DTRAX Bone Screw N/A
Completed NCT02081456 - Soft Tissue Mobilization Versus Therapeutic Ultrasound for Subjects With Neck and Arm Pain N/A
Terminated NCT00308594 - Oral Dexamethasone for the Treatment of Cervical Radiculopathy Phase 2
Completed NCT05887427 - Acute Effect of Neural Mobilization in Cervical Radiculopathy: A Randomized Controlled Study N/A
Completed NCT05852613 - Effect of HPLT on Pain and Electrophysiological Study in Cervical Radiculopathy Patients Phase 3