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OpenTrials
Completed

NCT Number: NCT01080287

The Identification and Characterization of Autonomic Dysfunction in Migraineurs With and Without Auras

This is a study to compare subject response and symptoms resulting from administration of three clinical assessments.

* The 3 assessments are

1. passive upright tilt table testing, 2. quantitative sudomotor axon reflex testing (QSART)and 3. punch biopsy.

The comparison of results will be from two subject groups:

* Group A, the migraine suffering patient with or without aura * Group B, the migraine suffering patient with or without aura who has diagnosed orthostatic intolerance (i.e.,feeling dizzy or faint when making a body position change).

Completed

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Cleveland Clinic NI, Center for Headache and Pain, Desk T-33, 9500 Euclid Avenue

Cleveland, Ohio, 44195, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age 18 to 65
  • male or female
  • migraine diagnosis
  • may or may not have orthostatic intolerance
  • able to demonstrate study understanding and complete informed consent process

Exclusion criteria

  • subjects who do not meet inclusion criteria
  • subjects unable to complete informed consent process

Sponsors and collaborators

Lead sponsor

The Cleveland Clinic

Other

Registry information

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Mar 4, 2010
Registry last updated
Feb 22, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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