Who we are
Ecto MD Clinical Trials delivers rigorous, patient-centered research designed to bring safer, more effective therapies to market — faster. We partner with patients, providers, and sponsors to run high-quality clinical trials across a wide range of therapeutic areas, combining clinical expertise, streamlined operations, and unwavering regulatory compliance.
What we do best
Expert study design and site management: Our clinical teams include experienced investigators, research nurses, and study coordinators who follow protocol precisely while keeping patient safety and comfort top of mind.
Rapid, efficient enrollment: We maintain active outreach programs and a growing database of interested volunteers, enabling prompt recruitment and reduced study start-up times.
Patient-first approach: We provide clear, compassionate communication, flexible visit scheduling, and supportive resources so participants can confidently complete study requirements.
Compliance and quality assurance: All trials are conducted under strict adherence to Good Clinical Practice (GCP), IRB oversight, and FDA/EMA regulatory standards. Robust data monitoring and secure systems protect participant information and study integrity.
Full-service capabilities: From Phase I through Phase IV studies, we handle site initiation, patient recruitment, informed consent, study visits, adverse event reporting, and data collection — delivering reliable results for sponsors.
Why partner with Ecto MD Clinical Trials
Faster enrollment and retention: Our proactive recruitment strategies and patient-focused operations minimize dropouts and keep studies on schedule.
Proven operational excellence: Experienced staff, standardized workflows, and continuous quality improvement translate to consistent, reproducible study conduct.
Trust and transparency: Participants receive clear information about risks and benefits and are treated with respect at every step; sponsors receive timely reports and open communication.
Flexible collaboration: We adapt to sponsor needs — whether single-site, multi-site, or decentralized trial models — and scale resources accordingly.
We are always looking for patients
Join studies that matter: Participants help advance new treatments for numerous conditions while receiving careful medical oversight and compensation for time and travel when applicable.
Easy to get started: Contact our team to discuss eligibility, available trials, and next steps. Our staff will guide you through screening and explain what to expect.
Support every step of the way: From initial contact through study completion, we provide thorough education, consistent follow-up, and a caring research environment.
Act now If you are a potential participant, healthcare provider, or sponsor interested in partnering with a dedicated, experienced clinical trials team, contact Ecto MD Clinical Trials today to learn about current studies and how we can work together to advance medical care.
Principal Investigator
Dr. David Othman, MD, is a board-certified dermatologist and micrographic dermatologic surgeon with over 10 years of clinical and surgical experience. He completed his MD at Northeast Ohio Medical University and dermatology training at Indiana University, where he served as Chief Resident. Dr. Othman has published in peer-reviewed journals, presented at national conferences, and teaches dermatology trainees at multiple Chicago-area programs.
Board-certified by the American Board of Dermatology, he is a fellow of the American Society for Dermatologic Surgery and the American Academy of Dermatology. He actively participates in clinical research and dermatology clinical trials, with experience in patient enrollment, protocol adherence, and investigator responsibilities.
Contact us
Interested in working together? Fill out some info and we will be in touch shortly. We can’t wait to hear from you!