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
- Diseases
- Cystic fibrosis
- 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
Sites (18)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of New Mexico Coordinator of this site? Confirm its status | Albuquerque | United States | Not yet recruiting |
| Emory University School of Medicine Coordinator of this site? Confirm its status | Atlanta | United States | Recruiting |
| University of Colorado Denver Coordinator of this site? Confirm its status | Aurora | United States | Recruiting |
| University of Alabama at Birmingham Coordinator of this site? Confirm its status | Birmingham | United States | Not yet recruiting |
| Massachusetts Coordinator of this site? Confirm its status | Boston | United States | Not yet recruiting |
| Medical University of South Carolina Coordinator of this site? Confirm its status | Charlestone | United States | Not yet recruiting |
| Baylor College of Medicine Coordinator of this site? Confirm its status | Houston | United States | Not yet recruiting |
| University of Iowa Coordinator of this site? Confirm its status | Iowa City | United States | Not yet recruiting |
| Keck Medical Center of USC Coordinator of this site? Confirm its status | Los Angeles | United States | Not yet recruiting |
| University of Miami Coordinator of this site? Confirm its status | Miami | United States | Not yet recruiting |
| University of Minnesota Coordinator of this site? Confirm its status | Minneapolis | United States | Recruiting |
| Tulane University Coordinator of this site? Confirm its status | New Orleans | United States | Not yet recruiting |
| Columbia University Cystic Fibrosis Program Coordinator of this site? Confirm its status | New York | United States | Not yet recruiting |
| Stanford University Coordinator of this site? Confirm its status | Palo Alto | United States | Not yet recruiting |
| The Children's Hospital Of Philadelphia Coordinator of this site? Confirm its status | Philadelphia | United States | Recruiting |
| The University of Texas Health Science Center at San Antonio Coordinator of this site? Confirm its status | San Antonio | United States | Recruiting |
| University of California San Diego Coordinator of this site? Confirm its status | San Diego | United States | Not yet recruiting |
| Atrium Health Wake Forest Baptist (Wake Forest Baptist) Coordinator of this site? Confirm its status | Winston-Salem | United States | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.