Studying the Presence of CFRD Complications With Thoughtful Recruitment (SPeCTRuM)

NCT ID: NCT06837181

Last Updated: 2026-01-22

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-09-18

Study Completion Date

2028-11-30

Brief Summary

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This multicenter cross-sectional study will include a diverse population of adolescents and adults with CF.

The overall Aim is to describe prevalence of diabetes microvascular complications and macrovascular surrogates in people with established CFRD.

Detailed Description

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Conditions

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Cystic Fibrosis (CF) Cystic Fibrosis-related Diabetes Diabetes Retinopathy Neuropathy Nephropathy Blood Pressure Cardiovascular Risk Microvascular

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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

Intervention Type OTHER

This is an observational study.

Interventions

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observational study

This is an observational study.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Written informed consent (and assent when applicable) obtained from participant or participant's legally authorized representative
* 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 any illness or condition that, in the opinion of the investigator might confound the results of the study or pose an additional risk to the subject
* 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.
Minimum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cystic Fibrosis Foundation

OTHER

Sponsor Role collaborator

Jaeb Center for Health Research

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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University of Colorado Denver

Aurora, Colorado, United States

Site Status RECRUITING

Emory University School of Medicine

Atlanta, Georgia, United States

Site Status RECRUITING

University of Iowa

Iowa City, Iowa, United States

Site Status NOT_YET_RECRUITING

University of Minnesota

Minneapolis, Minnesota, United States

Site Status RECRUITING

The Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

Site Status RECRUITING

The University of Texas Health Science Center at San Antonio

San Antonio, Texas, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Judy Sibayan, MPH, CCRP

Role: CONTACT

813-975-8690

Victoria Barnes-Lomen, MS

Role: CONTACT

813-975-8690

Facility Contacts

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Christine Chan, MD

Role: primary

720-777-6128

Tanicia Daley, MD MPH

Role: primary

404-727-2503

Katie Larson Ode, MD

Role: primary

319-356-4443

Amir Moheet, MD

Role: primary

617-624-3209

Andrea Kelly, MD

Role: primary

215-590-3174

Maria Rayas, MD

Role: primary

210-567-5283

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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