32 Paid Clinical Research Studies in Baltimore, Maryland

Filtered for protocols that accept healthy volunteers or mention compensation. Always confirm stipend details and screening with the study coordinator.

Interventional Protocol

The HOPE Study: Characterizing Patients With Hepatitis B and C

This is an observational, longitudinal, prospective study for sample collection and evaluation for future therapy or disease progression of chronic hepatitis B and C. Participants

πŸ“ Institute of Human Virology, University of Maryland School of Medicine β€” Baltimore, Maryland

πŸ’΅ In this sub-study, participants will receive an approved nucleos(t)ide analogue prospectively observed on therapy for ch

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Phase4

C-Raven, a Virtual Tobacco Cessation Intervention in Residency Clinics

In a residency clinic in Baltimore, the investigators propose to conduct a pilot RCT comparing a) an avatar-delivered computerized intervention (CI) for tobacco cessation augmented

πŸ“ Johns Hopkins University School of Medicine β€” Baltimore, Maryland

πŸ’΅ Intervention: Computer-Delivered Intervention (CDI) Session 1: Following the baseline assessment, participants will rec

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Phase2

Neoadjuvant Enoblituzumab (MGA271) in Men With Localized Intermediate and High-Risk Prostate Cancer

This study evaluates the safety, anti-tumor effect, and immunogenicity of Enoblituzumab given before radical prostatectomy. All patients will receive Enoblituzumab for 6 weekly dos

πŸ“ Johns Hopkins Sidney Kimmel Comprehensive Cancer Center β€” Baltimore, Maryland

πŸ’΅ All patients will receive Enoblituzumab for 6 weekly doses beginning 50 days prior to radical prostatectomy.

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Phase1 / Phase2

A Phase 1/2a to Evaluate the Safety and Efficacy of Adipose Tissue Allograft (BRC-OA) in Patients With Osteoarthritis of the Knee

The purpose of this study is to evaluate the safety profile of BRC-OA for pain treatment in patients with mild to severe OA of the knee, focusing particularly on two distinct doses

πŸ“ LifeBridge Health β€” Baltimore, Maryland

πŸ’΅ The initial 3 subjects will receive a 2 mL dose of BRCOA, and if deemed safe and well-tolerated by the investigator, the

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Phase1 / Phase2

Safety and Efficacy of the Bacteriophage Preparation, ShigActiveβ„’, in a Human Experimental Model of Shigellosis

The study is a first-in-human Phase 1/2a randomized, double-blind, placebo-controlled trial to assess the clinical safety and efficacy of ShigActive in healthy adults with experime

πŸ“ University of Maryland, Baltimore, University of Maryland School of Medicine, Center for Vaccine Development and Global Health β€” Baltimore, Maryland

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Observational / Diagnostic

Digital Literacy Intervention to Address Support, Literacy and Communication in Older Adults

The investigators propose a person-directed, values-based digital literacy intervention to address the community-identified barriers of health literacy, health communication and so

πŸ“ Johns Hopkins School of Nursing β€” Baltimore, Maryland

πŸ’΅ Each participant will receive 4-6 home visits with 3-4 interim phone calls based on the participant's individual digital

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Early Phase1

Analysis of the Microbiome in Rosacea

The skin and gut microbiome of rosacea patients differs from individuals without rosacea and that the microbiome suffers from unique derangements in rosacea patients following anti

πŸ“ Cutaneous Translational Research Program, Department of Dermatology β€” Baltimore, Maryland

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Phase2

Intravesical Gemcitabine and Docetaxel for BCG naΓ―ve Non-muscle Invasive Bladder Cancer

A single-arm, two-stage, open-label, phase 2 study investigating the safety and efficacy of intravesical gemcitabine/docetaxel for bacillus Calmette-Guerin (BCG)-naΓ―ve patients wit

πŸ“ Johns Hopkins University: Sidney Kimmel Comprehensive Cancer Center β€” Baltimore, Maryland

πŸ’΅ All participants will receive an induction course of gemcitabine/docetaxel instillations (administered once a week for s

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Observational / Diagnostic

Pain Self-Management and Treatment Engagement for Patients Taking Opioids

The goal of this study is to learn if Pain Self-Management (PSM) can improve chronic pain care in individuals with opioid misuse or opioid use disorder (OUD) The main questions it

πŸ“ Comprehensive Care Practice β€” Baltimore, Maryland

πŸ’΅ Participants will: * Take part in the PSM program or receive standard care for 12 weeks after enrolling in the study *

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Interventional Protocol

Impact of Ketogenic Diets on Cardiovascular Health in Adults With Epilepsy

This research is being done to evaluate the short term and long term effects of ketogenic diets on measures of cardiovascular health. Such measures include cholesterol levels, bloo

πŸ“ Johns Hopkins University β€” Baltimore, Maryland

πŸ’΅ If participants agree to be in this study, the investigators will ask the participants to do the following things: At I

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Phase2

Psilocybin Treatment of Major Depressive Disorder With Co-occurring Alcohol Use Disorder

The purpose of this study is to determine whether psilocybin, a hallucinogenic drug, is effective in reducing depressive symptoms and amount of drinking in patients with co-occurri

πŸ“ Johns Hopkins Center for Psychedelic and Consciousness Research β€” Baltimore, Maryland

πŸ’΅ After primary endpoints are measured, all volunteers will receive a second, unblinded intervention with a single high do

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Phase4

Vital Pulp Treatment in Primary Teeth

In primary teeth, decay that is near the pulp (tooth nerve)is treated with either a pulpotomy or indirect pulp treatment if the tooth is not going to be extracted A pulpotomy invol

πŸ“ University of Maryland School of Dentistry β€” Baltimore, Maryland

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Phase3

Behavioral Pharmacological Examination of a Novel Buprenorphine Induction Method Among Individuals Who Use Fentanyl

The opioid overdose epidemic has persisted for several decades and is now further complicated by the permeation of fentanyl into the illicit opioid supply. While the effectiveness

πŸ“ Johns Hopkins School of Medicine β€” Baltimore, Maryland

πŸ’΅ In a single-ascending dose design, the investigators will incrementally assess the tolerability of 4, 8, 16, and 24 mg o

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Phase1

DMID 23-0015; Lassa Fever CVD 1000

This study proposes the evaluation of a novel, first-in-human Lassa fever vaccine based on the complete Lassa glycoprotein complex (GPC) antigen. The antigen will be presented on a

πŸ“ University of Maryland, Baltimore, University of Maryland School of Medicine, Center for Vaccine Development and Global Health β€” Baltimore, Maryland

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Observational / Diagnostic

Behavioral Weight Loss for Cancer Survivors in Maryland: A Trial With Adaptive Interventions

The objective of the HELPLINE Weight Loss Program is to determine the comparative effectiveness of two active multi-component, augmented interventions for cancer survivors with ove

πŸ“ Johns Hopkins ProHealth β€” Baltimore, Maryland

πŸ’΅ Intensive Helpline in early non-responders (additional 6 months) All participants will receive * written Johns Hopkins

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Interventional Protocol

The Very Large Database of Lipids

Closer examination of granular lipid data in a large population offers numerous opportunities to generate new knowledge, ranging from studies examining concordance between commonly

πŸ“ Johns Hopkins University β€” Baltimore, Maryland

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Early Phase1

GLP-1 and Hypoglycemia

Low blood sugar can negatively affect how blood vessels function, and this can lead to an increase in the risk for heart attacks, strokes and other problems related to the stiffeni

πŸ“ University of Maryland, Baltimore β€” Baltimore, Maryland

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Phase4

Pain Self-Management and Patient-Oriented Dosing for Pain and in Retention Opioid Treatment

This study seeks to improve the treatment of chronic pain in people who are taking buprenorphine (also known as Suboxone, Subutex, Zubsolv). The research study is testing two diff

πŸ“ Alcohol and Drug Abuse Program (ADAP) - UM Addiction Treatment Center β€” Baltimore, Maryland

πŸ’΅ Participants will receive $50 compensation for each survey visit completed (up to $250 over one year) and can receive up

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