Wake Forest University Health Sciences
Wake Forest University Health Sciences sponsors 1,140 registered US clinical trials on ClinicalTrials.gov, 174 of them currently recruiting, and 724 completed. 111 of these trials are in Phase 3-4 (later-stage) and 239 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Breast Cancer, with 9 trials.
Trial Pipeline
1,140 total, page 6 of 23
Suzetrigine Frame Trial Comparing Suzetrigine and Acetaminophen
NCT07525219
Allograft vs. Autograft Nonunion
NCT07310082
Assessing Psoriasis Treatment Outcomes
NCT07391423
Patient Centered Simulation For Labor and Delivery
NCT03654079
Lumbar Drain With Intrathecal Nicardipine in Aneurysmal Subarachnoid Hemorrhage
NCT07246629
Assessing and Addressing Follow-up Care Needs That Will Facilitate Care Transitions for Cancer Survivors
NCT06654245
Comparing Technological and Relational Approaches to Support Families After a Missed Well Child Visit
NCT06686849
RCT-Consumer Perceptions of Cannabidiol (CBD) Health Claims
NCT06800066
A Randomized Controlled Trial to Test the Effects Oxytocin and Vibration Have on Heat Pain Threshold After UV-B Burn
NCT06651476
Using a Patient Navigator to Address the Social Drivers of Health in the Management of Pain
NCT06665906
Addressing Disparities in Diabetes Care
NCT06643611
Evaluation of Pharmacist Interventions in Lipid Management for Secondary Prevention
NCT06647238
Addressing Financial Hardship in Adolescent and Young Adult Cancer Survivors
NCT06881108
Evaluating Spinal Cord Stimulation for Stiff Person Syndrome
NCT06242678
GrowWell - Responsive Bottle Feeding
NCT06319807
Resident Posture Biofeedback Study
NCT06564519
Pedal Movement - Implementing Cycling as a Mobility Option
NCT06412991
A Portal-based Advance Care Planning Intervention Among Community-Dwelling Persons Living With Cognitive Impairment
NCT06509373
Investigating the Feasibility and Outcomes of Patient Self-Drain Removal After Ventral Hernia Repair
NCT06237855
Implementation of an Evidence-Based Intervention to Improve Head Impact Safety in Youth Football
NCT06368050
Text Intervention to Facilitate Secure Storage and Disposal of Prescription Opioids
NCT05503186
Education Session to Improve Program Adherence
NCT06428695
Va Meh Du Intervention
NCT06394193
Cannabis Edibles Packaging Imagery Experiment
NCT06358144
Relaxing Environment to Lower Anxiety During Onabotulinum Toxin Chemodenervation of the Bladder
NCT06319898
Sleep Well 24 (SWELL24) Healthy Sleep-Wake Behaviors in Older Adults
NCT05780983
Blood Flow Restriction Therapy Following Acute Shoulder Injury Patients
NCT06223373
Vivo Heart: Home-Based Virtual Exercise Program for Older Adults With Cardiovascular Disease
NCT05972850
Cannabis Edibles Packaging Descriptors Experiment
NCT06171399
Organization-level Youth Engagement Approach for Substance Misuse Prevention
NCT05736211
Anticipating Decline and Providing Therapy
NCT06182995
Storytelling To Prevent Obesity and Encourage Responsive Feeding Practices in Young Children
NCT05994924
Leveraging Social Innovation and Community-Engagement to Reduce Disparities in Outbreak Control Outcomes
NCT05123729
Pressure Relief Education and Training for Wheelchair Users
NCT06252597
Adapting a Sepsis Transition and Recovery Program for Optimal Scale Up
NCT05997420
ASPIRE: Adapting Self-Blood Pressure Monitoring to Reduce Health Disparities
NCT06175793
Temporary Peripheral Nerve Stimulation System for Osteoarthritis of the Knee
NCT06152029
Battlefield Auricular Acupressure (BAApress) Feasibility Study
NCT05939388
Cereset Research Long-Term Healthcare Worker Study
NCT05994261
Infracalcaneal Peppering Injection Technique for Chronic Plantar Fasciitis
NCT05868577
Consumer Perceptions of Cannabidiol (CBD) Health Claims
NCT06069713
A Comparison of the Outcomes in Fortiva and Strattice Mesh
NCT05572021
Tools for Anxiety and Depression Screening in Epilepsy
NCT05864612
Effect of Amifampridine on Neuromuscular Transmission in Patients Treated With OnabotulinumtoxinA
NCT05769478
Use of Dermabond in Mitigation of Spinal Cord Stimulation (SCS) Trial Lead Migration
NCT05914311
Feasibility of a Patient Directed Tool to Assess Heart Health Among Endometrial Cancer Survivors
NCT05796518
Implementation of a Mediterranean Diet Program for Overweight or Obese Pregnant Women in a Low-resource Clinical Setting
NCT05868954
Defining a PK and PD Model for Peripheral Analgesia After IV Oxytocin
NCT05929339
Perioperative Monitoring of Cardiac Surgery Patients With the Vitalstream Physiological Monitor
NCT05905536
Practice Patterns Among Gynecologic Oncologists on Tumor Genetic Testing in Endometrial Cancer
NCT05877404
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 96 |
| Phase 2 | 143 |
| Phase 3 | 31 |
| Phase 4 | 80 |
Therapeutic Areas
What the Pipeline for Wake Forest University Health Sciences Shows
According to the ClinicalTrials.gov registry, Wake Forest University Health Sciences is linked to 1,140 US clinical trials across every stage of research activity. Of those, 174 studies are currently recruiting, about 15% of the sponsor's indexed portfolio, and 724 are already marked complete, representing roughly 64% of the total.
The phase mix for Wake Forest University Health Sciences reports 111 late-stage studies (Phase 3 and Phase 4 combined) and 239 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Wake Forest University Health Sciences is Breast Cancer with 9 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.