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Cervicogenic Headache clinical trials

View clinical trials related to Cervicogenic Headache.

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NCT ID: NCT03919630 Completed - Clinical trials for Cervicogenic Headache

Mobilization Versus Manipulation for the Treatment of Cervicogenic Headaches

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

There is currently a gap within the literature as to the effects of a thrust versus non-thrust mobilizations techniques specifically to the upper cervical spine C0-C3 along with home exercise program to help reduce frequency and intensity of cervicogenic headaches. Therefore, the purpose of this study is to examine the effectiveness of in treating headaches using non-thrust or thrust mobilizations in addition to postural corrective exercises on patient outcomes measures.

NCT ID: NCT03478735 Completed - Clinical trials for Migraine Without Aura

Ultrasound Greater Occipital Nerve Block at C2 Level Compared to Landmark-based Greater Occipital Nerve Block

Start date: July 17, 2017
Phase: N/A
Study type: Interventional

This study will compare the analgesic benefit of a traditional landmark-guided GON block with the ultrasound-guided approach over a four week period in patients with occipital neuralgia or cervicogenic headache.

NCT ID: NCT03113357 Completed - Clinical trials for Cervicogenic Headache

The Effect of Myofascial Release in Patients With Cervicogenic Headache

RCT
Start date: January 2015
Phase: N/A
Study type: Interventional

Cervicogenic headache (CeH) is a secondary and often unilateral that is known by referring pain from soft or hard cervical structures to occipital, temporal, frontal and sometimes pre-orbital regions. There is higher prevalence of cervical muscle tightness, assessed clinically in CeH patients and anatomically there are some fascial connections between sub-occipital muscles with vertebra of C2 and Dura-mater.Therefore fascial restriction in this region can limit the normal movement of muscles between fascial plates in different directions in sub-occipital region. The purpose of current study was to compare the effect of MFR Technique in the upper cervical region with common (Exs) on pain intensity, frequency, duration and Pressure Pain Threshold (PPT) of upper cervical joints in subjects with CeH.

NCT ID: NCT01988363 Completed - Clinical trials for Cervicogenic Headache

Greater Occipital Nerve Injection Study

GON
Start date: June 2013
Phase: Phase 1
Study type: Interventional

This study is designed to answer the question of whether injection of the greater occipital nerve at its proximal origin, near the C2 vertebrae, using ultrasound guidance is effective in improving pain in human subjects. HYPOTHESES 1. Ultrasound (US) guided greater occipital nerve (GON) injections are effective at a novel, proximal C2 location in live, human subjects, measured by improvement in visual analog scale (VAS) pain scores pre-injection compared to VAS scores 30 minutes post-injection, 2-weeks post-injection, and 1-month post-injection . 2. Ultrasound (US) guided injection of the greater occipital nerve (GON) at a novel, C2 location is effective at improvement of both occipital neuralgia and cervicogenic headache demonstrated by improvement in visual analog scale (VAS) pain scores pre-injection compared to VAS scores 30 minutes post-injection, 2-weeks post-injection, and 1-month post-injection. We further hypothesize that the mean improvement in VAS scores at 1-month post injection will be greater than 2 units. 3. Ultrasound (US) guided injection of the greater occipital nerve (GON) at novel, proximal C2 location in live, human subjects appears safe.

NCT ID: NCT01790074 Completed - Clinical trials for Cervicogenic Headache

Trigger Point Therapy in Cervicogenic Headache

Start date: October 2010
Phase: N/A
Study type: Interventional

It is a pilot randomized controlled trial comparing real and simulated manual treatment of trigger points (TrPs) in patients with cervicogenic headache (CeH). The purpose of the current randomized clinical pilot trial was to determine the preliminary effects of TrP manual therapy in individuals with CeH with sternocleidomastoid muscle active TrPs as compared to manual contact over the muscle tissues.

NCT ID: NCT01687881 Completed - Clinical trials for Cervicogenic Headache

Is Chiropractic Spinal Manipulative Therapy an Efficient Treatment Option in Cervicogenic Headache

Start date: September 2012
Phase: N/A
Study type: Interventional

This study will highlight and validate chiropractic spinal manipulative therapy (CSMT) for cervicogenic headache (CEH). If the method proves to be effective, it will provide a new non-pharmacological treatment option for CEH. This is especially important since pharmacological management has minor effect in CEH, and alternative treatment options are warranted. The applied methodology of the study will aim towards the highest possible research standards. This international study is a collaboration between Akershus University Hospital, Innlandet Hospital and University of Oslo (UiO), Norway and Macquarie University, Australia. The multidisciplinary professional backgrounds are physiotherapy, chiropractic and medicine. By increasing the methodological quality of the investigators research to a very high level, the investigators see the method to work as a guide to increase the quality of chiropractic research in the future, as previous randomized clinical trials (RCTs) of CEH used methodology showing room for improvement. Study hypothesis: CSMT using the Gonstead method reduces days with CEH by at least 25% as compared to placebo (sham manipulation, i.e. broad non-specific contact, non-directional, low velocity and low amplitude) and no intervention (control group).

NCT ID: NCT01580280 Completed - Clinical trials for Cervicogenic Headache

Manual Therapy and Exercise in Patients With Cervicogenic Headache

Start date: April 2012
Phase: N/A
Study type: Interventional

Hypothesis: The group of cervicogenic headache patients receiving upper cervical and upper thoracic thrust manipulation will demonstrate significant and clinically important changes in outcomes when compared to the mobilization and exercise group.

NCT ID: NCT01530321 Completed - Clinical trials for Cervicogenic Headache

Cervicogenic Headache Dose-Response

CGH D-R
Start date: August 2012
Phase: Phase 1/Phase 2
Study type: Interventional

This study will determine the number of visits to a chiropractor for spinal manipulation and light massage necessary for the optimal relief of cervicogenic headache (headache with associated neck pain). Effectiveness of care will also be determined.

NCT ID: NCT00184197 Completed - Clinical trials for Cervicogenic Headache

Botulinum Toxin Injection in Neck Muscles in Cervicogenic Headache

Start date: May 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the effect and side-effects of injections with botulinum toxin in neck muscles in cervicogenic headache compared to injections with sodium water.