Clinical Trials Logo
  1. Home
  2. Rotator Cuff Tendinitis
  3. NCT04703660
  4. Details
NCT04703660 Clinical Trial

Effect of Cervical Mobilization on Rotator Cuff Tendinitis

Rotator Cuff Tendinitis Clinical Trial

Official title:
Immediate and Carry Over Effect of Different Cervical Mobilization Techniques on Rotator Cuff Tendinitis Patients

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04703660
Other study ID # interventional
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2021
Est. completion date June 1, 2021

Study information
Verified date May 2021
Source Egyptian Chinese University
Contact Noha S Elserty, PhD
Phone +201006709648
Email noha_elserty@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this study aimed to investigate the effect of 3 types of cervical mobilization on the strength of shoulder abductors, external rotators and pain level in patient with rotator cuff tendinitis. the measurement will be made immediately, 10 minutes, and 30 minutes after mobilization

Description:

subjects will be allocated according to the inclusion and exclusion criteria from outpatient clinic at El sahel teaching hospital. they will be assigned randomly into 3 groups, each group will receive certain type of cervical mobilization. the outcome measures will be measured before, immediate, 10 minutes, and 30 minutes after treatment

Recruitment information / eligibility
Status Recruiting
Enrollment 45
Est. completion date June 1, 2021
Est. primary completion date June 1, 2021
Accepts healthy volunteers No
Gender All
Age group 25 Years to 40 Years
Eligibility Inclusion Criteria: - patients will be included if they have rotator cuff tendinitis Exclusion Criteria: - Patients will be excluded if they had recent neck trauma or acute whiplash disorder ,any intra articular injection in the gleno-humeral joint during last three months, patients with musculoskeletal disorder (any type of fracture), any history of surgery on that shoulder and tendon calcification, cervical rib, rotator cuff tear.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• cervical mobilization
3 types of cervical mobilization at the level of C 5- 6

Locations
Country Name City State
Egypt Noha Elserty Cairo

Sponsors (1)
Lead Sponsor Collaborator
Noha Elserty

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary change in strength of shoulder abductors strength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder abductors before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization
Primary change in strength of shoulder external rotators strength testing with a hand-held dynamometer will be applied for 3 groups using Isometric contraction of shoulder external rotators before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization
Primary change in pain level pain severity will be measured using visual analogue scale for 3 groups before treatment, immediate, 10 minutes, and 30 minutes after cervical mobilization
See also
  Status Clinical Trial Phase
Withdrawn NCT03319784 - Analysis for NSAID VS Corticosteroid Shoulder Injection in Diabetic Patients Phase 4
Not yet recruiting NCT06023914 - Analysis of the Effect of Neuromuscular Electro-stimulation on the Performance of Isometric Rotator Cuff Strength. Phase 2/Phase 3
Completed NCT01984203 - Rotator Cuff Tendinopathy Exercise Trial N/A
Completed NCT01402011 - Study of 25% Dextrose Injections in Shoulder Ligaments and Tendons to Promote Their Healing N/A
Completed NCT01355549 - Platelet-Rich Plasma Therapy for Shoulder Pain in Persons With Spinal Cord Injury Phase 1
Terminated NCT00764764 - Study of the Effect of Neck Treatment on Shoulder Impingement Phase 1
Completed NCT03892603 - Does The Type of Exercise Influence Outcome in Rotator Cuff Related Shoulder Pain N/A
Active, not recruiting NCT03752827 - Autologous Adult Adipose-Derived Regenerative Cell Injection Into Chronic Partial-Thickness Rotator Cuff Tears N/A
Recruiting NCT05264935 - Ultrasound-guided Lavage of Calcific Deposits of the Rotator Cuff
Recruiting NCT02967640 - Does Subacromial Injection With Glutamate Receptor Antagonist, Ketamine, Attenuate Pain in Rotator Cuff Tendinopathy? Phase 2/Phase 3
Terminated NCT04115644 - Effectiveness of Corticosteroid vs. Ketorolac Shoulder Injections: A Prospective Double-Blinded Randomized Trial Phase 4
Completed NCT03425357 - Sonoelastography of the Supraspinatus Tendon N/A
Completed NCT03425344 - Discriminative Validity of Strain Elastography of the Supraspinatus Tendon N/A
Recruiting NCT04923477 - Therapeutic Exercise for Rotator Cuff Tendinopathy / Subacromial Pain Syndrome - Outcomes and Mechanisms N/A
Not yet recruiting NCT06372600 - Effect of Extracorporeal Shock Wave Combined With Autologous Platelet-rich Plasma Injection on Rotator Cuff Calcific Tendinitis N/A
Completed NCT06425913 - Effects of Cold and Kinesio Taping in Individuals With Rotator Cuff Tendonitis N/A
Completed NCT03675399 - Effect of Isometric Exercise on Pain Perception in Rotator Cuff Related Shoulder Pain N/A
Recruiting NCT05489484 - Performance and Safety Evaluation of MD-Shoulder Collagen Medical Device in the Treatment of Rotator Cuff Syndrome N/A
Recruiting NCT04094298 - Use of Extended Release Triamcinolone in the Treatment of Rotator Cuff Disease Phase 3
Active, not recruiting NCT03167138 - Micro-Fragmented Adipose Tissue (Lipogems®) Injection for Chronic Shoulder Pain in Persons With Spinal Cord Injury Early Phase 1