Last reviewed · How we verify

NCT04900493

The Rett Syndrome Global Registry

Recruiting now Last updated 17 February 2026
What this trial tests

trial in Rett Syndrome in 5,000 participants. Currently enrolling.

Timeline
31 January 2022
Primary endpoint
30 June 2031
30 June 2031

Quick facts

Lead sponsorRett Syndrome Research Trust
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment5,000
Start date31 January 2022
Primary completion30 June 2031
Estimated completion30 June 2031
Sites1 location across United States

Conditions studied

Sponsor

Rett Syndrome Research Trust

Who can join

Eligibility, any sex, with Rett Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The Rett Global Registry is a fully remote, global, caregiver-reported registry to collect information about caring for a loved one with Rett syndrome. In addition, caregivers have the ability to track and graph their loved one's symptoms and care strategies over time, store information for central access, and opt-in to complete medical record consolidation and summary. Qualified researchers and therapeutic developers may request access to de-identified aggregate information to further Rett research, or assist with clinical development planning to facilitate and expedite more effective clinical trials.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Rett Syndrome

Currently open trials in the same condition.

Other Rett Syndrome Research Trust trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04900493.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing