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The Will Erwin Headache Research Center - Cluster Headache Study (WEC1)

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Enrolling

Conditions

Paroxysmal Hemicrania
Trigeminal Neuralgia
Cluster Headaches and Other Trigeminal Autonomic Cephalgias
SUNCT
Hemicrania Continua
Cluster Headache

Study type

Observational

Funder types

Other

Identifiers

NCT02910323
HSC-MS-15-0780

Details and patient eligibility

About

The Will Erwin Headache Research Center Study of Cluster Headache and Trigeminal Neuralgia is a prospective, multicenter, observational research network for subjects with Cluster Headache and/or Trigeminal Neuralgia.

Full description

The Will Erwin Headache Research Center will assemble a national registry of Cluster Headache patients and will sub-categorize and organize this cohort based on individuating characteristics including but not limited to type and severity of condition, associated symptoms, and medical/psychological issues (e.g., depression, disability, sleep). Detailed evaluations and classification will be completed for each enrolled subject. This will encompass genomic and epigenomic studies, past medical history, imaging reports, and specific physical exam results for each patient. It will also enable the study investigators to match patients with suitable interventional clinical trials.

Similar diseases, such as other paroxysmal hemicrania, SUNCT, SUNA, hemicrania continua, and trigeminal neuralgia may also be investigated.

Enrollment

1,500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Diagnosis of a trigeminal autonomic cephalalgia according to the International Headache Classification including episodic cluster headache, chronic cluster headache, episodic paroxysmal hemicrania, chronic paroxysmal hemicrania, episodic short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT), chronic SUNCT, episodic short-lasting unilateral neuralgiform headache attacks with cranial autonomic symptoms (SUNA), chronic SUNA, and hemicrania continua. OR Diagnosis of a trigeminal neuralgia according to the International Headache Classification, including classical trigeminal neuralgia and symptomatic trigeminal neuralgia.
  • Able to provide HIPAA authorization to share prior medical records/imaging.

Exclusion criteria

  • Life expectancy less than 1 year, co-existing disease or other characteristic that precludes appropriate diagnosis of a trigeminal autonomic cephalalgia or trigeminal neuralgia.
  • Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements
  • Inability or unwillingness of subject or legal guardian/representative to give informed consent.

Inclusion Criteria for Healthy Volunteers:

  • Inclusion criteria is willingness to consent and be of age 18 and older

Trial design

1,500 participants in 2 patient groups

Experimental group
Description:
Patients with a history of Cluster Headaches and other TACs, or Trigeminal Neuralgia.
Family/Healthy Controls
Description:
Healthy volunteer controls and family members may be enrolled for identification of genetic mutations.

Trial contacts and locations

1

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Central trial contact

Rebecca Martinez, RN; Mark J Burish, MD, PhD

Data sourced from clinicaltrials.gov

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