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NCT01793168 · ClinicalTrials.gov registry record

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

A clinical trial of Rare Disorders and Cornelia de Lange Syndrome, sponsored by Sanford Health.

Recruiting
Registry status
20,000
Enrollment target
2
Study locations

NCT01793168: Recruiting study of Rare Disorders and Cornelia de Lange Syndrome, sponsored by Sanford Health.

NCT01793168 is a study of Rare Disorders and Cornelia de Lange Syndrome that is actively recruiting participants, run by Sanford Health. The registered enrollment target is 20,000 participants. The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01793168, a study of Rare Disorders and Cornelia de Lange Syndrome, is actively recruiting participants, sponsored by Sanford Health.

RECRUITING
Registry status
20,000 participants
Enrollment target
2
Study locations

Study Summary

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access. Visit sanfordresearch.org/CoRDS to enroll.

Study Locations (2)

South Dakota

  • Sanford Health - Sioux Falls

Other

  • Online Patient Enrollment System - Sydney

Trial Details

FieldValue
Enrollment Target 20,000 participants
Start Date 2010-07
Est. Completion 2100-12
Sanford Health

34 total trials

What NCT01793168 shows while recruiting

NCT01793168 is an observational study that tracks outcomes without assigning an intervention. Its 20,000 participants enrollment target places it among the larger protocols in the corpus.

The record links to 10 conditions, with Rare Disorders appearing as the primary indexed condition, and to 0 interventions.

NCT01793168 reports a single indexed study location in South Dakota, Other.

Frequently Asked Questions

What is clinical trial NCT01793168 about?

NCT01793168 is a clinical study titled "Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford". CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help a...

What is the current status of trial NCT01793168?

This trial is currently recruiting. The enrollment target is 20,000 participants. The study started on 2010-07. Estimated completion is 2100-12.

What conditions does trial NCT01793168 study?

This clinical trial studies the following conditions: Rare Disorders, Cornelia de Lange Syndrome, Undiagnosed Disorders, Disorders of Unknown Prevalence, Prenatal Benign Hypophosphatasia.

Who is sponsoring clinical trial NCT01793168?

This trial is sponsored by Sanford Health, which has 34 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01793168 being conducted?

This trial has 2 study locations across South Dakota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT01793168, the US trial registry maintained by the National Library of Medicine. NCT01793168 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.