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Combined Effect Of Cranial And Cervical Mobilization In Patients With CGH

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

Cervicogenic Headache

Treatments

Other: Mobilization Techniques
Other: Conventional Treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT05697445
Mobilization In CGH Treatment

Details and patient eligibility

About

  • 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

Enrollment

30 estimated patients

Sex

All

Ages

18 to 40 years old

Volunteers

No 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Cranial Mobilization and Exercises Group
Experimental group
Treatment:
Other: Conventional Treatment
Other: Mobilization Techniques
Exercises Group
Active Comparator group
Treatment:
Other: Conventional Treatment

Trial contacts and locations

0

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Central trial contact

Mennat Allah Hussien Mahmoud

Data sourced from clinicaltrials.gov

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