Actively Recruiting
Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility
Led by Brooklyn Clinical Research · Updated on 2024-06-11
10000
Participants Needed
1
Research Sites
254 weeks
Total Duration
On this page
AI-Summary
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.
CONDITIONS
Official Title
Triage Survey for Cardiovascular, Obesity, and Related Endocrine Trial Eligibility
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant or legally authorized representative has signed informed consent before any study procedures
- Participant is at least 18 years old
You will not qualify if you...
- Participant is pregnant, breastfeeding, or planning to become pregnant
- History of a clinically significant illness that may affect safety or study results
- Moderate or severe substance use disorder within 90 days prior to screening
- Any condition making the participant unsuitable for the study according to the investigator
- Currently employed by Swift Clinical Research Group, Inc. or related subsidiaries, or a first-degree relative of such an employee
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Brooklyn Clinical Research
Brooklyn, New York, United States, 11226
Actively Recruiting
Research Team
A
Ammara Mushtaq, MD
CONTACT
K
Katherine Azer, MS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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