Clinical trials

7

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Glucose Levels and Outcomes in Women - Mid Pregnancy

Up to 75% of reproductive age women are overweight, 40% are considered obese, and the prevalence of gestational diabetes mellitus (GDM) continues to rise, from 6% to 8.3% between 2016 and 2021. Currently understood GDM risk factors, such as advanced maternal age, prior history of GDM, family history of diabetes, and socioeconomic status can only explain up to 50% of cases. Related factors such as body image dissatisfaction, eating behaviors, and daily stress exposure have been linked to blood sugar metabolization, pregnancy outcomes, and the normative physiological changes that occur during pregnancy. These interrelated mechanisms may serve as additional risk factors that could help identify other women at risk of GDM. This project aims to investigate how body image dissatisfaction, eating behaviors, and daily stress exposure are associated with the metabolization of blood sugar during pregnancy. In this study the Strahm Lab will recruit 50 pregnant women to participate in a study assessing blood sugar metabolization as it is related to stress, body image dissatisfaction, and eating behaviors. The study will use continuous glucose monitoring in concert with an ecological momentary assessment protocol to assess these interrelated factors over the course of 10 days between 14 and 28 weeks gestation.

Participants needed: 50
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Sanford HealthUpdated: May 20, 2026Locations: 3
Eligibility criteria

At least 18 years old [+2]

history of diabetes [+4]

Status: Recruiting

Baseline ACL Injury Risk Screening and Normative Data

This is a prospective, observational cohort study aimed at establishing a database of normative biomechanics for healthy athletes and surveying these athletes for 12 months following baseline testing for the occurrence of new musculoskeletal injuries, with a particular emphasis on ACL injuries.

Participants needed: 5,000
Trial details
Age: 10-65Biological sex: AllType: ObservationalSponsor: Sanford HealthUpdated: Apr 17, 2026Locations: 1
Eligibility criteria

Healthy athletes participating in formal, organized, competitive sports between...

Status: Recruiting

Midwest Birth Outcomes and Indigenous American Pregnancy

Indigenous American pregnancies in the Midwest have disproportionally high rates of adverse outcomes, however little research has been done on how historical trauma and stress may impact these adverse outcomes. This project gathers data from pregnant Indigenous American women on their experiences with historical trauma, stress, and birth outcomes, as well as physiological data of how they respond to stress, in order to better understand the associations between these factors and the biological mechanisms underlying them. Understanding the mechanisms by which both historical and proximal stress "get under the skin" and influence pregnancy health and perinatal outcomes, will afford new targets of intervention to help reduce these IA health disparities.

Participants needed: 80
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Sanford HealthUpdated: Mar 20, 2026Locations: 2
Eligibility criteria

At least 18 years old [+3]

Assistive reproductive technology (in-vitro fertilization) [+1]

Status: Recruiting

General Population Level Estimation for Type 1 Diabetes Risk in Children During Routine Care Delivery

In partnership with Helmsley Charitable Trust, the Sanford PLEDGE Study is a large-scale, observational, feasibility study of general population screening for T1D and celiac autoantibodies. Screening is incorporated into routine health care visits within an integrated health system.

Participants needed: 33,000
Trial details
Age: 0-17Biological sex: AllType: ObservationalSponsor: Sanford HealthUpdated: Mar 2, 2026Locations: 4
Eligibility criteria

Newborn Entry: Viable, term infants, defined as 36 weeks gestation by either dat... [+4]

Subject is in the opinion of the investigator, unable to comply with the require... [+1]

Status: Recruiting

Opioids Versus Non-Opioids Postoperative After Knee Arthroscopic Surgery

The purpose of this study is to look at pain management with opioids versus non-opioids after knee arthroscopy. This study will determine 1) whether the most commonly used non-narcotic medications provide pain relief comparable with the most commonly prescribed narcotic medications in patients undergoing arthroscopic knee surgery, and 2) whether patients' characteristics (gender, pre-operative knee symptoms, workers compensation status and employment status) affect pain level following surgery or medication usage.

Participants needed: 148
Trial details
Phase: Phase 4Age: 18-80Biological sex: AllType: InterventionalSponsor: Sanford HealthUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Subjects ≥ 18 years of age through ≤ 80 years of age [+1]

Previously enrolled in this study (enrolled for contralateral knee in this study... [+17]

Status: Recruiting

Transcranial Direct Current Stimulation for Motor Function and Fatigue in PD

The investigators hypothesize that multi-session anodal tDCS (atDCS) of the left primary motor cortex (M1) will induce long-lasting effects in improving motor function and reducing motor fatigue and fatigability in PD patients.

Participants needed: 64
Trial details
Biological sex: AllType: InterventionalSponsor: Sanford HealthUpdated: Feb 3, 2026Locations: 1
Eligibility criteria

Clinical diagnosis of PD with at least two of the four diagnostic criteria for P... [+1]

Patients with dementia (MOCA < 21) [+6]

Status: Recruiting

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access. Visit sanfordresearch.org/CoRDS to enroll.

Participants needed: 20,000
Trial details
Biological sex: AllType: ObservationalSponsor: Sanford HealthUpdated: May 29, 2025Locations: 2Duration: 100 Years
Eligibility criteria

Diagnosis of a rare disease, a disease of unknown prevalence, undiagnosed or an...

Diagnosis of a disease which is not rare