GNAO1 Natural History Study

Status unconfirmed

Conditions studied: GNAO1

In brief

The purpose of the GNAO1 Natural History Study is to establish the clinical phenotype of GNAO1 associated neurologic disease, its association with genotype, and areas of clinical importance within the disease.

Key facts

Study ID

NCT04950946

Run by

Washington University School of Medicine

People needed

50

Starts

2019-02-18

Expected to finish

2022-12-01

Last updated by the study team

2021-07-06

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Enrollment in the Bow Foundation GNAO1 registry.
• Evidence of a known pathogenic mutation in GNAO1 or a variant of unknown significance and clinical symptoms likely to be consistent with GNAO1 as determined by study physicians.

You may not qualify if…

• Inability to obtain informed consent from parents or adult subjects.
• Inability to obtain medical records.

Where it is running

• Washington University School of Medicine — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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