Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility
Recruiting · NCT06412536 · Observational (researchers observe without assigning treatment) · Lead sponsor: Brooklyn Clinical Research
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
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.
Who can take part
Inclusion criteria
- Participant or Legally Authorized Representative has signed an ICF prior to study-specific procedures being performed.
- Participant is at least 18 years old.
Exclusion criteria
- Participant is pregnant, breast-feeding, or planning to become pregnant.
- History of a clinically significant illness which in the investigator's opinion may impact participant safety or the ability to analyze study results.
- Moderate or severe substance use disorder within 90 days prior to screen
- Any condition that in the investigator's opinion makes a participant unsuitable for the study.
- 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.
Where it is running
2 locations listed across 1 US state.
- Brooklyn Clinical Research - Brooklyn, New York, United States
- Brooklyn Clinical Research - Brooklyn, New York, United States