Studying the Presence of CFRD Complications With Thoughtful Recruitment (SPeCTRuM)
NCT ID: NCT06837181
Last Updated: 2026-01-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
200 participants
OBSERVATIONAL
2025-09-18
2028-11-30
Brief Summary
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The overall Aim is to describe prevalence of diabetes microvascular complications and macrovascular surrogates in people with established CFRD.
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Individuals with Cystic Fibrosis-Related Diabetes
Individuals diagnosed with Cystic Fibrosis-Related Diabetes for more than 5 years before enrollment
observational study
This is an observational study.
Interventions
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observational study
This is an observational study.
Eligibility Criteria
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Inclusion Criteria
* For Adults: Must be able to consent on one own's behalf (i.e., cannot lack cognitive capacity to consent due to the required patient-reported outcomes)
* Be willing and able to adhere to the study protocol requirements
* Age ≥ 12 years at time of enrollment
* CF diagnosis based on two CF causing mutations and/or positive sweat test according to CFF diagnostic criteria
* CFRD diagnosis ≥ 5 years at time of enrollment
Exclusion Criteria
* History of transplant
* Pregnancy reported by participant at time of consent or at any point during active study participation
* Erratic, accelerated or mechanically controlled irregular heart rhythms including arrhythmias
* Carotid or aortic valve stenosis
* Peripheral artery disease or leg artery disease
* Generalized constriction or localized spasm of muscular conduit arteries such as seen immediately after hypothermic cardiopulmonary bypass surgery or accompanying Raynaud's phenomena or intense cold.
* Possible exclusions based on investigator medical provider assessment (additional precautions may be followed to allow inclusion):
* Pressure reading should not be conducted on a limb where there is intravenous access, arterio-venous shunt, or where circulation is compromised.
* Pressure reading should not be conducted on the side of the body that a mastectomy was done.
12 Years
ALL
No
Sponsors
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Cystic Fibrosis Foundation
OTHER
Jaeb Center for Health Research
OTHER
Responsible Party
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Locations
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University of Colorado Denver
Aurora, Colorado, United States
Emory University School of Medicine
Atlanta, Georgia, United States
University of Iowa
Iowa City, Iowa, United States
University of Minnesota
Minneapolis, Minnesota, United States
The Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
The University of Texas Health Science Center at San Antonio
San Antonio, Texas, United States
Countries
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Central Contacts
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Facility Contacts
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References
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Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
007365A124
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
SPeCTRuM
Identifier Type: -
Identifier Source: org_study_id
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