Rare condition

Oculocerebral hypopigmentation syndrome, Cross type

ORPHA:2719 ↗Malformation syndrome

45

studies recruiting now

as of 7 Sept 2026

587

studies registered in total

as of 7 Sept 2026

3

countries with a recruiting site

as of 7 Sept 2026

11 Aug 2026

most recent study posted

among recruiting studies

Recruiting trials

RecruitingNot applicableNCT07677111

Chronotype Alignment and Time Perception

Sponsor The Hong Kong Polytechnic UniversityWhere Hong Kong (1 site)Studying Morning test session (about 08:00), Evening test session (about 22:00)Updated 30 Jun 2026

Showing the 5 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.

See all 45 recruiting studies

Where recruiting studies are running

Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.

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Patient organisations

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About Oculocerebral hypopigmentation syndrome, Cross type

RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations.

Related conditions

Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).