Combined Effect Of Cranial And Cervical Mobilization In Patients With CGH

Combined Effect Of Cranial And Cervical Mobilization In Patients With Cervicogenic Headache

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05697445

Enrollment

Registered

2023-01-25

Start date

2023-02-28

Completion date

2023-09-30

Last updated

2023-02-01

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

Conditions

Cervicogenic Headache

Brief summary

* The purposes of this study are: * To investigate the combined effect of cranial and cervical mobilization in patient with cervicogenic headache and there effect on : 1. Perceptive neck pain intensity 2. Perceptive headache intensity 3. pain by pressure 4. frequency of headache episodes 5. duration of headache episodes 6. Medications uptakes

Interventions

OTHERMobilization Techniques

Combination of Cranial and Cervical Mobilization for Cervicogenic headache Patients treatment

OTHERConventional Treatment

Cervicogenic headache exercises

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 40 Years

Healthy volunteers

Inclusion criteria

* pain originating at the neck and radiating to oculo-frontal-temporal regions. * symptom unilaterally. * symptom provocation through cervical movement and/or awkward cervical postural. * symptom provocation through external pressure application through palpation to associated posterior cervical spine segments with resultant symptom reproduction. * possible ipsilateral shoulder and/or arm pain of vague reference. * 15 or more headache episodes per month * No history of cervical operation or any disease that result in headache as colities -All patients will sign the informed consent before joining the study.

Exclusion criteria

* Headache not of cervical origin * Headache with autonomic involvement, dizziness, or visual disturbance * Congenital conditions of the cervical spine * It is of primary concern to exclude serious or life-threatening pathology such as : * cranial tumors. * Meningitis. * sub-arachnoid hemorrhage. * carotid artery,vertebral artery dissection. * History of cervical operation or any disease that result in headache as colitis * Age less than 18 or more than 40 years * chronic maxillary sinusitis

Design outcomes

Primary

Measure	Time frame	Description
Assis Headache Perceptive intensity	2 weeks	By visual analog scale , Minimum value zero mean No pain Maximum value 10 mean Worst pain .

Contacts

Primary ContactMennat Allah Hussien Mahmoud

mena.elkatatny80c@gmail.com+2001090122467

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026