Traction Manipulation of Upper Cervical Spine on Cervicogenic Dizziness
NCT ID: NCT02772042
Last Updated: 2018-05-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
40 participants
INTERVENTIONAL
2015-10-31
2017-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of C0-C1 Mobilization in the Neutral Position in Subjects With Upper Cervical Rotational Hypomobility
NCT02404766
Effects of Pain, Disability and Cervicokinesthesia After Cervical Manipulation
NCT02645630
Effect of Rotatory Upper Cervical Manipulation on Reflex Cervical Vertigo
NCT05002296
Clinical Effects of Upper Cervical Translatoric Mobilization in Patients With Headache
NCT02422862
Comparison of Two Spinal Manipulation Treatments in Patients With Chronic Mechanical Neck Pain
NCT04268667
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention Group
Investigators will performed traction manipulation of those articulations of upper cervical spine with indication for this treatment. Before manipulation soft tissue techniques will be applied in order to prepare the joint. After manipulation the patient rest in supine position. The intervention will have a duration of 10 minutes.
Intervention Group
Control Group
The patient of the control group maintain the supine position for 10 minutes.
Control Group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Intervention Group
Control Group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Hypomobility of upper cervical spine.
* Sing the informed consent form.
Exclusion Criteria
* Pending litigation or legal claim.
* Poor language and communication skills making difficult to understand the informed consent.
18 Years
85 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Andoni Carrasco
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Andoni Carrasco
PT
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Andoni Carrasco, Pt
Role: PRINCIPAL_INVESTIGATOR
Unidad de Investigación en Fisioterapia. Universidad de Zaragoza
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Unidad de Investgación en Fisioterapia. Universidad de Zaragoza
Zaragoza, , Spain
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PI15/0230
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.