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NCT06837181Recruiting

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

Source: ClinicalTrials.gov · Last updated 10 Feb 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
29 Jan 2025
Start date
18 Sept 2025
Primary completion date
30 Nov 2028
Lead sponsor
Jaeb Center for Health Research
NCT number
NCT06837181

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 18 Sept 2025 to the primary completion date, 30 Nov 2028
  • 18 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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.

Other illness

  • 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
  • Erratic, accelerated or mechanically controlled irregular heart rhythms including arrhythmias
  • Peripheral artery disease or leg artery disease

Other

  • Pregnancy reported by participant at time of consent or at any point during active study participation
    • Pulse Wave Velocity Exclusion Criteria:
  • Carotid or aortic valve stenosis
  • 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.

Who the study is looking for

  • 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

Age in the registry: 12 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (18)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of New Mexico
Coordinator of this site? Confirm its status
AlbuquerqueUnited StatesNot yet recruiting
Emory University School of Medicine
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting
University of Colorado Denver
Coordinator of this site? Confirm its status
AuroraUnited StatesRecruiting
University of Alabama at Birmingham
Coordinator of this site? Confirm its status
BirminghamUnited StatesNot yet recruiting
Massachusetts
Coordinator of this site? Confirm its status
BostonUnited StatesNot yet recruiting
Medical University of South Carolina
Coordinator of this site? Confirm its status
CharlestoneUnited StatesNot yet recruiting
Baylor College of Medicine
Coordinator of this site? Confirm its status
HoustonUnited StatesNot yet recruiting
University of Iowa
Coordinator of this site? Confirm its status
Iowa CityUnited StatesNot yet recruiting
Keck Medical Center of USC
Coordinator of this site? Confirm its status
Los AngelesUnited StatesNot yet recruiting
University of Miami
Coordinator of this site? Confirm its status
MiamiUnited StatesNot yet recruiting
University of Minnesota
Coordinator of this site? Confirm its status
MinneapolisUnited StatesRecruiting
Tulane University
Coordinator of this site? Confirm its status
New OrleansUnited StatesNot yet recruiting
Columbia University Cystic Fibrosis Program
Coordinator of this site? Confirm its status
New YorkUnited StatesNot yet recruiting
Stanford University
Coordinator of this site? Confirm its status
Palo AltoUnited StatesNot yet recruiting
The Children's Hospital Of Philadelphia
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesRecruiting
The University of Texas Health Science Center at San Antonio
Coordinator of this site? Confirm its status
San AntonioUnited StatesRecruiting
University of California San Diego
Coordinator of this site? Confirm its status
San DiegoUnited StatesNot yet recruiting
Atrium Health Wake Forest Baptist (Wake Forest Baptist)
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.