Triage Survey for Infectious Disease Eligibility
Brooklyn Clinical Research · NCT06492187
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Observational
- Target enrollment
- 10000
- US sites recruiting
- 1
- Study start
- June 28, 2024
- Record last updated
- July 9, 2024
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
SWIFT-ID-101 is a single site survey study designed to assess potential participants' eligibility to screen for industry-sponsored clinical trials for diagnosis, treatment, or prevention of infectious diseases such as in the areas of HIV, vaccines, and other infectious-diseases areas. A physician will oversee the informed consent process, after which participants will be surveyed on demographics, medical/surgical history, physical examination, comorbidities, and any current symptoms. Informed consent will be done electronically (preferable) or on paper. Informed consent may be done in-person or remotely, depending on patient preference. Information related to HIV, hepatitis B and C, other infectious diseases, or substance use disorder will also be obtained if applicable. Site staff may collect vital signs, fingerpick testing, urine drug screens, blood draws, EKG, and pregnancy tests. Some testing may be recommended in a fasting condition. A doctor will review medical history and results of the above evaluations with the participant to determine study suitability via clinical interview. The doctor may reach out to the patient's current treating physicians, other providers, and pharmacies to determine eligibility for clinical trials. A follow-up phone call may be needed to discuss testing results and/or trial eligibility. If a participant is deemed eligible for future trials and if the participant remains interested, counseling on contraception requirements for trials will be discussed.
Conditions: Vaccination; Infection; HIV-1-infection; Infectious Disease
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 1. 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
- Participants are 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 or makes them unsuitable for the study for another reason.
- Current or recent moderate or severe substance use disorder impacting their ability to follow study related procedures.
- Reported history of coagulopathy or bleeding disorder considered a contraindication to phlebotomy.
- Any condition that in the investigator's opinion makes a participant unsuitable for the clinical trial 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.
Recruiting US locations
Brooklyn Clinical Research
Brooklyn, NY 11226
Site contact: Ammara Mushtaq, MD · 929-203-5879 · amushtaq@brooklynclinicalresearch.com
Study contacts (from the official record)
- Ammara Mushtaq, MD · 9292035879 · amushtaq@brooklynclinicalresearch.com
- Katherine Azer, MS · 9293327848 · kazer@brooklynclinicalresearch.com
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