NCT06412536Recruiting
Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility
Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility (SWIFT-CORE-101)
Source: ClinicalTrials.gov · Last updated 11 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
SWIFT-CORE-101 is a single site survey study designed to assess potential participants' eligibility to screen for industry-sponsored clinical trials. A physician will oversee the informed consent process, after which participants will be surveyed on demographics, medical history, comorbidities, and current symptoms. Site staff may collect vital signs, urine drug screens, blood draws, and urine pregnancy tests. A doctor will review medical history with the participant to determine study suitability via clinical interview. The doctor may reach out to the patient's current treating physicians and pharmacies to determine eligibility for clinical trials.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 10000 (estimated)
- First submitted
- 6 May 2024
- Start date
- 30 May 2024
- Primary completion date
- 10 Apr 2029
- Lead sponsor
- Brooklyn Clinical Research
- Diseases
- Obesity, Type 2 diabetes
- NCT number
- NCT06412536
What you commit to
- Study type: Observational
- Planned participants: 10000
- From 30 May 2024 to the primary completion date, 10 Apr 2029
- 1 site 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
- Moderate or severe substance use disorder within 90 days prior to screen
Other illness
- History of a clinically significant illness which in the investigator's opinion may impact participant safety or the ability to analyze study results.
- Any condition that in the investigator's opinion makes a participant unsuitable for the study.
Other
- Participant is pregnant, breast-feeding, or planning to become pregnant.
- Currently employed by Swift Clinical Research Group, Inc. or any of its subsidiaries, including Brooklyn Clinical Research, or a first-degree relative of an employee.
Who the study is looking for
- Participant or Legally Authorized Representative has signed an ICF prior to study-specific procedures being performed.
- Participant is at least 18 years old.
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Brooklyn Clinical Research Coordinator of this site? Confirm its status | Brooklyn | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.