Research at Digestive Health Partners

For nearly three decades, Digestive Health Partners (DHP) has been advancing the field of gastroenterology through clinical research.
Research-Leading the Way

Leading the Way

Since 1996, our team has participated in more than 250 clinical trials, serving as a top site for academic centers, industry sponsors, and patients across Western North Carolina.

Our mission is simple: bring innovative treatments, devices, and techniques to our patients while helping move science forward. As the largest gastrointestinal and hepatology research department in North Carolina, and one of the largest in the Southeast, we combine intellectual curiosity, clinical expertise, and strict adherence to GCP/ICH guidelines to ensure integrity, quality, and meaningful results.

Contact Coordinator

If you have a gastrointestinal or liver disorder and are interested in learning more about a clinical research study in which you may be eligible to participate, please contact us.

Meet Our Research Director

DHP’s research program is led by Dr. William R. Harlan, III, who has directed or co-directed clinical research for more than 17 years. His career-long commitment to advancing clinical trial design and conduct has made DHP a respected leader in gastroenterology research.

Dr. Harlan and our team of certified coordinators, regulatory specialists, and clinical staff maintain the highest ethical standards and professional certifications, including GCP/ICH and CITI. Together, they provide patients with expert oversight and sponsors with clean, high-quality data.

Dr. William R. Harlan, III

Director of Research

Why Clinical Trials Matter

Clinical trials are essential to developing new therapies, devices, and approaches that improve patient care. At DHP, trials help us:

  • Test new treatments: Including drugs, biologics, and medical devices.
  • Prevent disease: Exploring vaccines, supplements, and lifestyle strategies.
  • Improve screening: Finding better ways to detect GI conditions earlier.
  • Enhance quality of life: Studying approaches to improve daily living for those with chronic illness.

Patient participation is voluntary but may provide benefits such as early access to promising treatments, closer monitoring, and free or subsidized trial-related care. Every study follows a strict informed consent process to ensure patients understand both risks and benefits.

Our Research Capabilities

We offer full-service, in-house capabilities that make participation and trial execution seamless.

These resources allow us to manage everything from complex GI procedures to advanced biologic therapies with efficiency and integrity.

On-Site Facilities

  • Endoscopy center with upper & lower endoscopy (MAC anesthesia if needed)
  • Dedicated exam rooms and research lab space
  • IV infusion therapy, PillCam, BRAVO, Fibroscan®, manometry, pH monitoring, breath testing

Lab & Data Resources

  • Secure EMR access, specimen processing, refrigerated/freezer storage
  • 12-lead ECG, calibrated centrifuges, temperature-monitored equipment
  • Digital file transfer, high-speed internet, data mining for feasibility

Why Clinical Trials Matter

  • Coordinators and regulatory specialists certified by ACRP (CCRC) and SoCRA (CCRP)
  • BLS/ACLS trained nurses and clinical staff
  • Extensive experience with protocol review, IRB submissions, recruitment, product storage/tracking, and case report completion through various EDC systems

For Office or Procedure Appointments

New Patients

Step 1: Ask your primary care provider to send us a referral.

Step 2: Once we receive it, our scheduling team will contact you and send you a secure patient portal link

Current Patients

Log in to your Patient Portal to schedule online using your username and password.

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