Recruiting

CoRDSCollection of Sociodemographic and Health Information for Rare Diseases Research

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

This study aims to connect individuals diagnosed with a rare disorder or those undiagnosed with researchers studying rare diseases, in order to accelerate research in this field.

What is being collected

Data Collection

Collected from today forward - Prospective
No Sample Retained
Who is being recruted

Congenital Abnormalities+301

+ Abnormalities, Multiple

+ Ciliopathies

+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: July 2010
See protocol details

Summary

Principal SponsorSanford Health
Study ContactCoRDS TeamMore contacts
Last updated: May 29, 2025
Sourced from a government-validated database.Claim as a partner

Study start date: July 1, 2010

Actual date on which the first participant was enrolled.

CoRDS collects contact, sociodemographic and health information about participants. This information is entered into CoRDS and linked to a unique coded identifier. Below are some examples of information requested on the Questionnaire that will be entered into CoRDS: Contact information: Name, Mailing Address, Phone Number, Email Address Sociodemographic information: Date of Birth, Place of Birth, Sex, Gender, Ethnicity Health information: Family History, Information related to Diagnosis De-identified information in CoRDS will be made available to researchers, if they have obtained approval for their research project from (1) the Institutional Review Board (IRB) at the researcher's institution and (2) a panel of experts. A subset of de-identified information collected from each profile may be shared with certain other databases. This is done in order to help improve understanding of rare diseases, to avoid the duplication of efforts and to collaborate with existing research efforts with organizations dedicated to rare diseases. Participants may elect to have their information shared with patient advocacy groups (PAGs) representing individuals with rare or uncommon diseases who have partnered with CoRDS. The PAG will sign an agreement stating that they will not use the information for Research purposes. CoRDS personnel will not be held responsible for the use of information by the PAG. The CoRDS Registry will not be paid by Researchers, Other Patient Registries or Patient Advocacy Groups (PAGs) for access to information in CoRDS. If a parent/LAR consents on behalf of a minor, CoRDS will contact the participant when he or she reaches the age of 18 in order to obtain consent. If this consent is not obtained in a timely manner, the participant will be withdrawn from CoRDS. CoRDS contacts participants annually to confirm continued interest in participation in CoRDS, and to request that participants update the information they have provided.

NCT01793168
Principal SponsorSanford Health
Study ContactCoRDS TeamMore contacts
Last updated: May 29, 2025
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

20000 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Congenital AbnormalitiesAbnormalities, MultipleCiliopathiesVector Borne DiseasesSynucleinopathiesPrimary Immunodeficiency DiseasesAortic Valve DiseaseNeuroinflammatory DiseasesUrogenital DiseasesCytopeniaImprinting DisordersAdrenal Gland DiseasesAdrenal InsufficiencyAmino Acid Metabolism, Inborn ErrorsAmnesiaAnemiaAnemia, HemolyticAortic Valve StenosisArterial Occlusive DiseasesAutoimmune DiseasesAutonomic Nervous System DiseasesBacterial Infections and MycosesBacterial InfectionsBasal Ganglia DiseasesMental DisordersBile Duct DiseasesBiliary Tract DiseasesBlood Platelet DisordersBone DiseasesBone Diseases, DevelopmentalBone Diseases, MetabolicBorrelia InfectionsBrain DiseasesBrain Diseases, MetabolicCarbohydrate Metabolism, Inborn ErrorsCardiovascular DiseasesCarotid Artery DiseasesCentral Nervous System DiseasesCentral Nervous System InfectionsCerebellar AtaxiaCerebellar DiseasesCerebral Arterial DiseasesCerebrovascular DisordersCholestasisCholestasis, IntrahepaticChronic DiseaseColonic DiseasesConnective Tissue DiseasesCranial Nerve DiseasesDeglutition DisordersDementiaDemyelinating DiseasesDigestive System AbnormalitiesDigestive System DiseasesDiseaseDwarfismDysostosesEar DiseasesEndocrine System DiseasesEndocrine Gland NeoplasmsEsophageal DiseasesEye AbnormalitiesEye DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsFibrosisFistulaGastrointestinal DiseasesGonadal DisordersHearing DisordersHeart Defects, CongenitalHeart DiseasesHeart Valve DiseasesHematologic DiseasesHemic and Lymphatic DiseasesHemolytic-Uremic SyndromeImmunologic Deficiency SyndromesImmune System DiseasesIntestinal DiseasesIntestinal FistulaIntestinal ObstructionIris DiseasesKidney DiseasesKidney Failure, ChronicKidney NeoplasmsKyphosisLipid Metabolism, Inborn ErrorsLipidosesLiver CirrhosisLiver DiseasesLymphatic DiseasesMalabsorption SyndromesMegacolonMemory DisordersMeningitisIntellectual DisabilityMetabolic DiseasesMetabolism, Inborn ErrorsMetal Metabolism, Inborn ErrorsMovement DisordersMuscle HypertoniaMuscular Atrophy, SpinalMuscular DiseasesMuscular DystrophiesMusculoskeletal AbnormalitiesMusculoskeletal DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesNeoplasmsNeoplasms by Histologic TypeNeoplasms by SiteNeoplasms, Multiple PrimaryNeoplasms, Muscle TissueNeoplastic Syndromes, HereditaryWilms TumorNerve Compression SyndromesNervous System MalformationsNervous System DiseasesNervous System NeoplasmsNeurologic ManifestationsNeuromuscular DiseasesNutritional and Metabolic DiseasesOptic AtrophyOptic Nerve DiseasesOtorhinolaryngologic DiseasesParaneoplastic SyndromesPathologic ProcessesPeripheral Nervous System DiseasesPolyneuropathiesPolyradiculoneuropathyPostoperative ComplicationsRectal DiseasesRetinal DegenerationRetinal DiseasesSarcomaScleroderma, SystemicSensation DisordersDisorders of Sex DevelopmentSigns and SymptomsSigns and Symptoms, DigestiveSkin DiseasesSleep Wake DisordersSphingolipidosesSpinal Cord DiseasesSpinal CurvaturesSpinal DiseasesSpirochaetales InfectionsPathological Conditions, Signs and SymptomsTelangiectasisThrombocytopeniaUremiaUrogenital AbnormalitiesUrogenital NeoplasmsUrologic DiseasesUrologic NeoplasmsUveal DiseasesVascular DiseasesVasculitisVirus DiseasesEsophageal Motility DisordersPyruvate Metabolism, Inborn ErrorsHereditary Sensory and Motor NeuropathyOptic Atrophies, HereditaryRenal Tubular Transport, Inborn ErrorsHistiocytosisHistiocytosis, Non-Langerhans-CellEye Diseases, HereditaryDigestive System FistulaLysosomal Storage DiseasesMotor Neuron DiseaseGram-Negative Bacterial InfectionsTick-Borne DiseasesSkin and Connective Tissue DiseasesSkin Diseases, VascularNeoplasms, Complex and MixedNeoplasms, Connective and Soft TissueCardiovascular AbnormalitiesPeroxisomal DisordersNeurodegenerative DiseasesNeurobehavioral ManifestationsNeurocognitive DisordersLysosomal Storage Diseases, Nervous SystemAmino Acid Transport Disorders, InbornHeredodegenerative Disorders, Nervous SystemAutoimmune Diseases of the Nervous SystemHereditary Central Nervous System Demyelinating DiseasesParaneoplastic Syndromes, Nervous SystemNeuromuscular Junction DiseasesBrain Diseases, Metabolic, InbornNeurocutaneous SyndromesPathological Conditions, AnatomicalIntracranial Arterial DiseasesCentral Nervous System Viral DiseasesDyskinesiasNeuromuscular ManifestationsSleep Disorders, IntrinsicDyssomniasMuscular Disorders, AtrophicDisease AttributesAortic Stenosis, SupravalvularChromosome DisordersGenetic Diseases, InbornHearing LossX-Linked Intellectual DisabilityGenetic Diseases, X-LinkedMannosidase Deficiency DiseasesIleusDNA Repair-Deficiency DisordersRenal Insufficiency, ChronicRenal InsufficiencyLipid Metabolism DisordersSulfatidosisFemale Urogenital DiseasesMale Urogenital DiseasesPrimary DysautonomiasOsteochondrosisSpinal OsteochondrosisLeukoencephalopathiesUrea Cycle Disorders, InbornThrombotic MicroangiopathiesProteostasis DeficienciesFrontotemporal Lobar DegenerationTDP-43 ProteinopathiesDisorder of Sex Development, 46,XYRetinal DystrophiesCauda Equina SyndromeOlivary DegenerationAddison DiseaseAtaxiaAtaxia TelangiectasiaBeckwith-Wiedemann SyndromeBiliary AtresiaCockayne SyndromeCystinosisDe Lange SyndromeDeafnessEsophageal AchalasiaFriedreich AtaxiaGlycogen Storage DiseaseHalitosisHirschsprung DiseaseDisorders of Excessive SomnolenceHypophosphatasiaInfectionsIntestinal Pseudo-ObstructionKlippel-Feil SyndromeLeigh DiseaseLeiomyosarcomaLeukodystrophy, MetachromaticLiver Cirrhosis, BiliaryLyme DiseaseMeningitis, ViralMoyamoya DiseaseMucocutaneous Lymph Node SyndromeMucolipidosesMuscle SpasticityMyasthenia GravisMyoclonusNarcolepsyMultiple Endocrine NeoplasiaNeuronal Ceroid-LipofuscinosesHereditary Sensory and Autonomic NeuropathiesOculocerebrorenal SyndromeHyperacusisRectal FistulaRefsum DiseaseRetinitis PigmentosaScheuermann DiseaseShort Bowel SyndromeSpinocerebellar DegenerationsSyndromePyruvate Dehydrogenase Complex Deficiency DiseaseLambert-Eaton Myasthenic SyndromeAniridiaAlagille SyndromeKleine-Levin SyndromeWAGR SyndromeMachado-Joseph DiseaseMultiple Endocrine Neoplasia Type 1Multiple Endocrine Neoplasia Type 2aMultiple Endocrine Neoplasia Type 2bWilliams SyndromeMultiple System AtrophyHyperglycinemia, NonketoticHyperargininemiaIdiopathic HypersomniaAmnesia, Transient GlobalSpinocerebellar AtaxiasMyasthenia Gravis, NeonatalMitochondrial DiseasesOptic Atrophy, Autosomal DominantDenys-Drash SyndromeRare DiseasesCoffin-Lowry SyndromeMuscular Dystrophy, Oculopharyngealbeta-MannosidosisScleroderma, DiffuseLymphohistiocytosis, HemophagocyticFrasier SyndromeWolf-Hirschhorn SyndromeBulbo-Spinal Atrophy, X-LinkedAlstrom SyndromeLeber Congenital AmaurosisFrontotemporal DementiaNeglected DiseasesAtypical Hemolytic Uremic Syndrome

Criteria

1 inclusion criteria required to participate
Diagnosis of a rare disease, a disease of unknown prevalence, undiagnosed or an unaffected carrier of a rare/uncommon disease

1 exclusion criteria prevent from participating
Diagnosis of a disease which is not rare

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

Recruiting

Sanford Health

Sioux Falls, United StatesOpen Sanford Health in Google Maps
Recruiting

Online Patient Enrollment System

Sydney, Australia
Recruiting
2 Study Centers