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NCT05002296 Clinical Trial

Effect of Rotatory Upper Cervical Manipulation on Reflex Cervical Vertigo

Vertigo Clinical Trial

Official title:
Effect of Rotatory Upper Cervical Manipulation on Reflex Cervical Vertigo in Chronic Mechanical Neck Pain Patients

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05002296
Other study ID # P.T.REC/012/002663
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 15, 2021
Est. completion date October 2021

Study information
Verified date August 2021
Source Cairo University
Contact ramy Salama draz, lecturer
Phone 00201111534173
Email dr.ramy.salama@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cervical reflex vertigo is a non-common cause of vertigo, caused by decreased afferent input from the upper three cervical segments to vestibular nuclei.

Recruitment information / eligibility
Status Recruiting
Enrollment 40
Est. completion date October 2021
Est. primary completion date September 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 60 Years
Eligibility Inclusion Criteria: - cervical pain - vertigo Exclusion Criteria: - severe osteoporosis - blood circulation problem

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• upper cervical manipulation
rotatory upper cervical manipulation to both sides. The treatment program was conducted for twelve sessions (three sessions per week). Assessment procedures were performed before and after treatment through visual analogue scale (VAS)

Locations
Country Name City State
Egypt faculty of physical therapy Cairo university Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain intensity seems to be improved Assessment procedures were performed before and after treatment through visual analogue scale (VAS) 3 monthes
Primary vertigo seems to be significantly improved Dix-Hallpike test was used to asses the vertigo degree and improvement within and after the treatment programme 3 monthes
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