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Transient Global AmnesiaPROTOSNCT06903026

PRevalence Of Transient Global Amnesia in Obstructive Sleep Apnea Syndrome

An observational study of Transient Global Amnesia, run by University Hospital, Strasbourg, France at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Amnesic stroke is an amnestic syndrome lasting less than 24 hours characterized by the occurrence of anterograde amnesia often associated with retrograde amnesia, the pathophysiology of which is still poorly understood at present. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Transient Global Amnesia
How many people
250 participants
Where
1 siteFrance
Study dates
17 Mar 2023to 31 Dec 2025
Phase
Observational
Are there results?
Not yet: the study is under way

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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients seen for consultation in the Neuropsychology Department of Strasbourg University Hospital between March 1, 2015 and December 31, 2021 following an episode of amnestic stroke meeting the Hodges and Warlow criteria.

Who may be able to join

  • Adult patients seen for consultation in the Neuropsychology Department of Strasbourg University Hospital between March 1, 2015 and December 31, 2021 following an episode of amnestic stroke meeting the Hodges and Warlow criteria:
  • The stroke must have been documented and reported by a competent witness present during the stroke.
  • Anterograde amnesia during the stroke.
  • Absence of vigilance, personality, and cognitive disorders other than memory disorders (aphasia, apraxia, etc.).
  • Absence of focal neurological symptoms during the episode and its aftermath.
  • Absence of epileptic manifestations.
Show all 9Show fewer
  • Resolution of the episode in less than 24 hours.
  • Exclusion of patients with a history of recent head trauma or active epilepsy (undergoing regular treatment or having experienced a seizure in the last 2 years).
  • Subjects who have not expressed opposition to the reuse of their data for scientific research purposes.

Who cannot join

  • Patients who have expressed opposition to the retrospective reuse of their data for scientific research purposes.
  • Patients with active epilepsy
  • Patients with recent head trauma
  • Patients with an MMS < or equal to 25
  • Subject under guardianship or curatorship
  • Subject under judicial protection

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

France1 site, 1 recruiting
  • Service de Neurologie - CHU de Strasbourg - France

    Strasbourg, 67091

    Benjamin CRETIN, MD, 33 3 88 12 86 34, benjamin.cretin@chru-trasbourg.fr

    Benjamin CRETIN, MD

    Recruiting

Other trials in France

About this study

Amnesic stroke is an amnestic syndrome lasting less than 24 hours characterized by the occurrence of anterograde amnesia often associated with retrograde amnesia, the pathophysiology of which is still poorly understood at present. A recent study on a small sample size (N=29) highlighted an association between obstructive sleep apnea syndrome and amnesic stroke. Our study seeks to confirm or refute these results on a larger cohort (N=200-250). A better understanding of the pathophysiological processes involved would open up new therapeutic avenues.

Keywords
Transient Global Amnesia, Sleep apnea syndrome
Medical subject headings
Amnesia, Transient Global, Sleep Apnea Syndromes

What is being measured

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

  1. To assess the prevalence of obstructive sleep apnea syndrome in patients who have experienced an amnestic stroke.

    Presence or absence of obstructive sleep apnea syndrome reported by a witness present during the stroke.

    Measured: Within the last 2 years

Timeline

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

  1. First posted30 Mar 2025
  2. Study start17 Mar 2023
  3. Primary completionDec 2025 (estimated)
  4. Study completion31 Dec 2025 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Case only
Time perspective
Retrospective
Enrolment
250 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06903026
Sponsor's protocol ID
8781
Acronym
PROTOS
Status last verified
Mar 2025
First submitted
24 Mar 2025
Last updated
30 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Transient Global Amnesia, run by University Hospital, Strasbourg, France at 1 site in France.

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 9 inclusion and 6 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: looking for participants now, as of the sponsor's last update on 30 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

This study is still under way. Results are not available in the source record yet.

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

Contact Benjamin CRETIN, MD (33 3 88 12 86 34, benjamin.cretin@chru-trasbourg.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To assess the prevalence of obstructive sleep apnea syndrome in patients who have experienced an amnestic stroke. (time frame: Within the last 2 years). 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 30 Mar 2025.

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