Clinical Research

Improving Patient Care & Advancing Medical Research

Sanford Health fosters a culture of innovative discovery through cutting-edge clinical trials.

We’re actively working to advance treatments and evidence-based care. Clinical trials give patients access to new treatments and help improve care for current and future generations.

Trials at Sanford Health focus on:

  • Improving the standard of care
  • Finding better ways to detect and prevent disease
  • Improving comfort and quality of life for patients

Anyone who meets the eligibility requirements can participate in a trial. Eligibility requirements may include age, sex, health and risk factors.

We offer trials at every stage of care, including:

  • Prevention
  • Diagnosis and screening
  • Treatment
  • Quality of life and condition management
  • Survivorship

Sanford Health’s clinical trials portfolio is driven by dedicated working groups. Each group provides direction for the development and oversight of a therapeutic area, ensuring the right clinical trials are offered to our patients. Working groups are led by physician experts, clinical research leadership, clinical investigators, clinical research professionals and leaders from health care services.

Browse our catalog of clinical trials to find a trial that’s relevant to you.


Clinical Research Trial Phases

Our trials are conducted across all phases of clinical research, including:

  • Phase 0: Discovery and lab-based research
  • Phase 1: Safety
  • Phase 2: Safety and dosing
  • Phase 3: Safety and efficacy
  • Phase 4: Post-approval surveillance

Protecting Patient Rights

Sanford Health’s Institutional Review Board (IRB) is a key component of our Human Research Protection Program and protects the rights, safety and well-being of participants.

Clinical Research News

Decentralized Clinical Trials

Expanding care access and enhancing research

Our decentralized clinical trials (DCTs) program brings clinical research opportunities closer to patients – especially those in rural areas – through technology and local partnerships. This approach enhances patient access, experience and engagement while maintaining the same regulatory and scientific standards as traditional clinical trials.


What are decentralized clinical trials?

DCTs are trials that use digital tools, remote monitoring and local clinical partnerships to conduct study-related activities outside of traditional research centers. Through DCTs, study participants receive expanded access to research-based care without having to travel a great distance.

Patients who participate in a DCT are typically referred by their provider. Arrangements are made with the patient regarding how they will receive their care for the trial, like through virtual visits at home or in a clinic.

Please contact our team if you need more information or would like to make a proposal.