Clin2
NCT04133272Likely a fitRecruiting

Registry for Ehlers-Danlos syndrome patients and pregnancies

Ehlers-Danlos Syndrome

Part of Blood & lymphatic, Genetic & congenital, Heart & circulation, Skin clinical trials.

This study is a registry that collects information about people with Ehlers-Danlos syndrome, including unborn babies diagnosed before birth. It may help researchers learn more about the condition and improve care over time.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
3,000 people
Ages
Any age
Study type
Observational

Who can take part

  • You have (or are expecting) a diagnosis of Ehlers-Danlos syndrome
  • The condition must be related to Ehlers-Danlos syndrome
  • If pregnant, your baby must have an Ehlers-Danlos diagnosis during pregnancy
  • You can be included even if you were diagnosed before birth
  • No other unrelated health condition should be the main reason for joining

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT06336473Not yet recruiting
Does cross-linking improve skin strength in Ehlers-Danlos syndrome?

This study tests whether a chemical cross-linking treatment can change the stretchiness and strength of skin in people with classic or hypermobile Ehlers-Danlos syndrome. Small skin samples will be taken to study the effects in the lab.

Paris
NCT06443346Recruiting
Registry for people with eosinophilic esophagitis

This is a registry (like a medical diary) for people with EoE who are getting regular treatment. It helps doctors track how EoE affects people over time, so they can improve care for everyone.

Milan, Lombardy
NCT05328050Recruiting
Registry for people with achondroplasia or hypochondroplasia

This is a research registry that enrolls people with achondroplasia or hypochondroplasia. It helps researchers collect information about the condition to improve understanding and future studies.

Milan
NCT04115774Recruiting
Registry for people with osteogenesis imperfecta

This study is a registry, meaning it collects health information about people with osteogenesis imperfecta (OI) to better understand the condition. It may help researchers learn what care works best and how OI varies from person to person.

Bologna, Emilia-Romagna
NCT04133285Recruiting
Registry for people with multiple bone growths

This study is a registry that collects information about people with multiple osteochondromas (extra bone/cartilage growths). It may help researchers better understand the condition and improve future care, even if no treatment is given.

Bologna, Emilia-Romagna
NCT07151274Recruiting
Ehlers-Danlos syndrome and women's gynecological health

This study uses an online questionnaire to explore how Ehlers-Danlos syndrome (EDS) may affect gynecological health. It compares women with EDS to those without, to better understand any differences.

Rouen

Hear when a new Ehlers-Danlos Syndrome trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.