Become a Healthcare

Current Clinical Research Studies

Heart Health Study

Must be over the age of 40 and living with obesity, or have been diagnosed with cardiovascular disease. Join our study to learn more about developing a healthy lifestyle!

Nosebleed Cessation Study

Must be 18 years of age or older to participate in the nosebleed cessation study. Must frequently experience nosebleeds (seasonal or non-seasonal) to be considered as a candidate.

Sprain & Strain Study

If you or your child are between the ages of 6-45 and have recently experienced a soft tissue injury, this study might be for you. Children must have a parent or legal guardian accompany them for all occurrences.

Asthma Study

Must be at least 12 years old to participate in the study. Must have a concern, medical diagnosis or other breathing-related symptoms that indicate the possibility of asthma or breathing disorder.

Atrial Fibrillation Study

Are you over the age of 18 and were diagnosed with atrial fibrillation within the last 90 days? You may qualify for participation in our study for treatment of irregular heart rhythms!

The Next Level Experience - Our Misson

Next Level Medical Clinical Research is a part of Next Level Urgent Care Clinics located throughout Houston, Austin, San Antonio, & Beaumont Texas area, thus providing a proliferating patient database, 44 well-established urgent care centers, and a trusted reputation within all of our communities. We’re able to provide a large-scale and highly diversified subject population and in doing so, continuously achieve high volunteer recruitment and retention by focusing on our mission of patient-customer centricity.

Since Next Level’s Clinical Research inception of clinical research in 2020, we have successfully conducted and managed clinical trials ranging in multiple therapeutics areas at our primary Tanglewood-Houston facility. Our urgent care centers are located throughout multiple cities enabling the ability to conduct decentralized and/or hybrid clinical trials when warranted to meet the needs of our customers and subject volunteer participants. Throughout our partnerships, we have exhibited resulted oriented successful outcomes by meeting or exceeding our targeted randomization goals, achieving 98% enrollment goals, 98% subject retention rate, and a 2% screen failure ratio

Next Level Medical Clinical Research comprehends the vast significant undertaking of clinical research. We are committed to providing the highest standard of agility, quality results oriented data, and participant care. With a combined experience of over 20 years in clinical research; our dedicated staff of principal investigators are board certified physicians with all applicable certifications such as GCP. Our clinical coordinators hold certifications in HIPPA, GCP and IATA with advanced degrees in areas of BSN-registered nurse, biology, clinical research, and organizational management.

Why Participate in Clinical Trials?

Our mission is to conduct safe and effective clinical trials to advance development of new medications. It is healthcare heroes like you who make new treatments possible. By participating in a clinical trial you may benefit from new investigational treatments that are not otherwise available to the public. As a participant in the clinical trial, no health insurance is required. You will receive free medical care from expert physicians and all study-related medical exams, laboratory tests, and procedures are provided at no charge. You will receive care from expert physicians and all study-related medical exams, lab tests, and procedures at no charge to you.

You may receive compensation for your time.

There is no cost associated with the visit or medication.

Conveniently located at our Tanglewood Clinic.

Steps for Participation and FAQs

Screening interview: Information will be taken concerning your age, medical history, medications, and other preliminary questions to make sure you meet the study requirements.

Assessments & Medication: Once you are enrolled in a study, you may have a study-related physical exam, receive the study medications, undergo laboratory tests, and other study procedures. During the course of the study, research team members will meet with you regularly to monitor your progress.

Informed Consent: You will receive materials that fully explain the nature of the study and how you will participate. Our research staff will tell you of any known risks or potential side effects. It is very important that you ask questions and read the consent form carefully. Please ask any questions you might have to fully understand the risks and benefits of your participation.

What is a clinical trial?

A clinical trial is medical research to study the safety and effectiveness of an investigational drug or device. The US Food and Drug Administration (FDA) uses information gathered in clinical trials to evaluate medications before approving them for use in the United States.

What do I need to know before a clinical trial?

Before you are evaluated as a research participant, we will provide you with an approved Informed Consent Form (ICF) which you must read, understand, and sign before enrolling. The ICF outlines all procedures you will need to go through and all known risks and side effects of the investigational medication. Please read it carefully and ask all questions you might have.

What is the risk in volunteering for a clinical trial?

Before conducting a clinical trial, pharmaceutical companies must obtain approval from the FDA to ensure that the investigational medication is appropriate to give to people. Additionally, all study procedures are reviewed by an independent Investigational Review Board (IRB) before they are allowed to be administered. All this is done to ensure that the study is ethical and that the risks are as low as possible. However, since the study participants are among the first to try the investigational medication, the risk of unanticipated side effects does exist. This is why the health of the people participating in the trials is continuously monitored and any serious side effects experienced by any of the people in the trial are promptly investigated. If necessary, corrective actions, including termination of the trial, are taken.

Do I qualify to participate?

Different studies have different enrollment requirements. Some studies are open only to healthy adults, other look for people with specific medical conditions, for instance, anxiety, depression, migraines, sexual dysfunction, etc. To determine whether you can enroll, we will ask several questions about your current health, your medical condition, and the medications you are taking. If you meet the study requirements, an appointment will be schedule for you to be evaluated in person.

Can I change my mind?

Your participation in a research study is entirely voluntary, and you may withdraw from participation at any time and for any reason. During your screening visit and throughout the study, we will fully explain the risks and benefits of your study. If you change your mind, you may withdraw.

Will my information be sold?

Any information you provide as a research participant is strictly confidential. It will not be sold and will be used only for the purposes of contacting you for relevant research studies.

Meet the Team!

WILNER JEUDY, MD: INVESTIGATOR

GCP, HSR, IATA, ACLS, BLS, CRIO, Veeva Vault CMDS, Medidata Classic Rave EDC

KATHERINE MCELROY, MD: INVESTIGATOR

GCP, HSR, RCR, IATA, ATLS, ACLS, BLS, CRIO

TAYLOR DAO: CLINICAL RESEARCH COORDINATOR

GCP, ASCLS PACE, IATA, CRIO, CRA, CIO, Social and Behavioral Responsible Conduct of Research, Veeva Vault CMDS

MICKO SANFORD: DIRECTOR OF RESEARCH

GCP, HSR, RCR, IATA, ACRP-CP, FIBRO SCAN

LAURA SANTANA: LEAD CLINICAL COORDINATOR

GCP, ASCLS PACE, IATA, CRIO, Veeva Vault CMDS, Medidata Classic Rave EDC

Next Level in Clinical Research

Next Level is partnering with key stakeholders in clinical research that are committed to pushing boundaries of science to deliver life-changing medical breakthroughs and therapies for all patients.

3 Exam Rooms

CLIA Certified Laboratory

Internal Quality Control

Utilize Sponsor Designated Central IRB

Central Location With Engagement Across Houston, Austin & San Antonio

12+ Years of Experience With Phase II - IV Trials

2 GCP Certified Investigators and 5 Sub-Investigators

IP Storage With 2-8°C Refrigerators & -20 to -70°C Freezers

Our clinical trial recruitment and outreach process incorporates a variety of engagement avenues, from leveraging our existing patient database, physician referral network, and even by way of digital, print, and social media marketing. We’re also partnered with both primary care and urgent care services to drive not just recruitment, but patient retention.

Previous Research Studies Conducted

RESPIRATORY TRIALS

Clinical Performance Evaluation of a Point of Care Test to Detect Antibodies to SARS-CoV-2.
Phase 2, Double-blind, Randomized, Placebo-Controlled Study of NasoVAX in the Prevention of Clinical Worsening in Patients with Early Coronavirus Infectious Disease 2019 (COVID-19).
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study Assessing the Efficacy and Safety of Anti-Spike SARS CoV-2 Monoclonal Antibodies in Preventing SARS-CoV-2 Infection in Household Contacts of Individuals Infected with SARS CoV-2.
A Phase III Randomized, Double-blind, Placebo-controlled, Multicenter Study to Determined the Safety and Efficacy of AAZD7442 for the treatment of COVID-19 in Non-Hospitalized Adults (TACKLE).
A Randomized, Double-blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy and Safety of LY38119253 and LY3832479 in Participants with Mild to Moderate COVID-19 Illness.
A Phase 2 Multiple Dose Study to Evaluate the Efficacy and Safety of PUL-0472 Inhalation Solution in Reducing the Severity of COVID-19 in Adults Positive for SARS-CoV-2 Infection.
A Phase 2 Multiple Dose Study to Evaluate the Efficacy and Safety of PUL-042 Inhalation Solution in Reducing the Infection Rate and Progression to COVID-19 in Adults Exposed to SARS-CoV-2.
An Interventional, Efficacy, and Safety, Phase 2, Randomized, Double-Blind, 2-Arm Study to Investigate A Repeat 5-Day Course of Nermatrelvir/Ritonavir compared to Placebo/Ritonavir in participants at least 12 years of age with Rebound of COVID-19 Symptoms and Rapid Antigen Test Positivity.
A Study of Acute Respiratory Infections in Global Outpatient Setting (ARGOS).
A Phase 2b, Double-Blind, Randomized, Placebo-Controlled, Parallel Group, Dose Ranging Study to Evaluate Virological Response and Safety of Oral PF_07817883 in Non-Hospitalized Symptomatic Adult Participants with COVID-19.

NEUROLOGY TRIALS

A Study of Donanemab Versus Placebo in Participants at Risk for Cognitive and Functional Decline of Alzheimer’s Disease.
A Phase 3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study, to Evaluate the Safety and Efficacy of SB-01 For Injections for the Treatment of Lumbar Degenerative Disc Disease.

CARDIOVASCULAR TRIALS

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Effect of Tirzepatide on the Reduction of Morbidity and Mortality in Adults with Obesity.

MUSCULOSKELETAL TRIALS

The Evaluation of a Nasal Compression Device in Comparison to Digital Nasal Compression for Stopping Epistaxis.
A Multi-Center, Prospective, Open-Label, Controlled Study of the Pharmacokinectics and Safety of the LicartTM Topical System in Pediatric and Adult Participants with Minor Soft Tissue Injuries.

GASTROINTESTINAL TRIALS

A Prospective, Multi-Center, observational Study for Signal-C Test Evaluation (PROMISE).

INFECTIOUS DISEASES TRIALS

POC SARS-CoV-2 Diagnostic PCR Device Comparison to FDA Approved Reference PCR Test.
Clinical Performance Evaluation of a Point of Care Test to Detect Antibodies to SARS-CoV-2.
POC SARS-CoV-2 Diagnostic PCR Device Comparison to FDA Approved Reference PCR Test.
A Randomized, Double-blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy and Safety of Mono and Combination Therapy with Monoclonal Antibodies in Participants with Mild to Moderate COVID-19 Illness (BLAZE-4).
An Interventional Phase 2/3, Adaptive, Multi-center, Randomized, Double-Blind Study to Investigate Efficacy and Safety of Oral Sisunatovir Compared with Placebo in Non-Hospitalized Symptomatic Adults with Respiratory Syncytial Virus Infections Who Are at Risk of Progression to Severe Illness.
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of GS-5245 for the Treatment of COVID-19 in Non-hospitalized Participants.
A Master Protocol Assessing the Safety, Tolerability, and Efficacy of Anti-Spike(s) SRS-CoV-2 Monoclonal Antibodies for the Treatment of Ambulatory Patients with COVID-19.