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Cervicogenic HeadacheNCT05697445

Combined Effect Of Cranial And Cervical Mobilization In Patients With CGH

A study testing Mobilization Techniques and Conventional Treatment in people with Cervicogenic Headache, run by Cairo University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 40 years
Conditions the study is for
Cervicogenic Headache
What is being tested?
Mobilization Techniques and Conventional Treatment
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
No sites listed yet
Study dates
Feb 2023to Sep 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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.

Who cannot join

  • 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.
Show all 11Show fewer
  • 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 locations and contacts

No sites are listed yet.

Mennat Allah Hussien Mahmoud contact

+2001090122467

mena.elkatatny80c@gmail.com

About this study

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

  • 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
Being tested
Mobilization Techniques, Conventional Treatment
Medical subject headings
Post-Traumatic Headache

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mobilization TechniquesOther

    Combination of Cranial and Cervical Mobilization for Cervicogenic headache Patients treatment

  • Conventional TreatmentOther

    Cervicogenic headache exercises

Study groups in NCT05697445
Study groupRoleWhat they receive
Cranial Mobilization and Exercises GroupExperimentalNot described
Receives: Other: Mobilization Techniques; Other: Conventional Treatment
Exercises GroupActive comparatorNot described
Receives: Other: Conventional Treatment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Assis Headache Perceptive intensity

    By visual analog scale , Minimum value zero mean No pain Maximum value 10 mean Worst pain .

    Measured: 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Jan 2023
  2. Study startFeb 2023 (estimated)
  3. Primary completionAug 2023 (estimated)
  4. Study completionSep 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05697445
Sponsor's protocol ID
Mobilization In CGH Treatment
Status last verified
Jan 2023
First submitted
29 Dec 2022
Last updated
1 Feb 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Mobilization Techniques and Conventional Treatment in people with Cervicogenic Headache, run by Cairo University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 1 Feb 2023. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Mennat Allah Hussien Mahmoud (+2001090122467, mena.elkatatny80c@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assis Headache Perceptive intensity (time frame: 2 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Feb 2023.

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