Wake Forest University
Wake Forest University sponsors 100 registered US clinical trials on ClinicalTrials.gov, 7 of them currently recruiting, and 74 completed. 22 of these trials are in Phase 3-4 (later-stage) and 15 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Urinary Incontinence, with 2 trials.
Trial Pipeline
100 total, page 2 of 2
A Comparison of Different Ventilation Strategies in Infants Using the PLMA™
NCT03235817
Early Provision of Enteral Microlipid and Fish Oil to Infants With Enterostomy
NCT01306838
Standardized Rehabilitation for Intensive Care Unit (ICU) Patients With Acute Respiratory Failure
NCT00976833
Physical and Cognitive Function - Look AHEAD Ancillary Study
NCT01410097
Tetracaine Combined Spinal Epidural (CSE) Versus Bupivacaine CSE
NCT01005459
Xience V at Wake Forest University Baptist Medical Center (WFUBMC)
NCT00937573
A Novel Method to Improve Acne Outcomes
NCT01176955
The Effect of Levocetirizine on Inflammatory Mediators in Dermatographism
NCT01008592
Adherence to Study Medication Compared to Generic Topical Clindamycin Plus Generic Topical Tretinoin in Subjects With Mild to Moderate Acne Vulgaris
NCT01047189
Pegaptanib Therapy in Non-Infectious Uveitic Cystoid Macular Edema
NCT00790803
Exercise Intolerance in Elderly Patients With Diastolic Heart Failure
NCT00959660
A 5 Year Follow-up on Newly Diagnosed Breast Cancer Patients
NCT01176838
Epidural Neostigmine for Labor Pain
NCT00779467
The Effects of Music Therapy on Women's Anxiety Before and During Cesarean Delivery
NCT01049477
Fixation of Unstable Distal Radius Fractures
NCT00654615
Long-Term One Year Use of Alefacept (Amevive®) in Moderate to Severe Chronic Plaque Type Psoriasis
NCT00655564
Measuring Adherence to Topical Therapy in Children With Atopic Dermatitis and the Impact of a Return Visit
NCT00654355
Effect of Spinal Ketorolac on Mechanical Hypersensitivity After a Total Hip Replacement
NCT00621530
Ethnic Differences in Response to Topical Capsaicin: A Psychophysical Study on Healthy Subjects
NCT00655811
Three Way Interaction Between Gabapentin, Duloxetine, and Donepezil in Patients With Diabetic Neuropathy
NCT00619983
Rhubarb and Angiotensin Converting Enzyme Inhibitor
NCT00672451
Effect of Spinal Ketorolac After Acute Opioid Exposure
NCT00693160
Efficacy of Desonide (Desonatetm) Gel 0.05% in Younger and Older Subjects With Atopic Dermatitis
NCT00690833
Severity Postoperative Pain Prediction
NCT00638404
Effect Of Acute Inflammatory Mediators On Functional Limitations In Patients With Acute Respiratory Failure
NCT01707303
Physical Activity Program for Older Renal Transplant Candidates
NCT00857974
Compatibility of a Mild, Moisturizing Hand Cleanser for Patients With Mild to Moderate Hand Dermatitis
NCT00843466
Evaluation of Scalp and Hair Shaft With Biologic Markers in African American and Caucasian Hair
NCT00690664
Measuring Adherence To Topical 5-Fluorouracil in a Clinic Population
NCT00696488
Structural Analysis of Human Tissue
NCT01293864
Comprehensive Investigation of Heart Rate Variability as a Measure of the Autonomic Nervous System in Atopic Dermatitis
NCT00691366
Adherence to Topical Hydrocortisone 17-butyrate 0.1% (Locoid®) Using Different Vehicles in Adults With Atopic Dermatitis
NCT00693693
Comparative Study of the Efficacy of SARNA Sensitive Lotion for Treatment of Uremic Itch in Adult Hemodialysis Patients
NCT00693654
Clinical Trial to Evaluate Biafine Cream Versus Standard Care in Subjects With Actinic Keratosis Post Cryotherapy
NCT00695578
Intensive Diet and Exercise for Improving Knee Osteoarthritis in Obese and Overweight Older Adults
NCT00381290
Measuring Adherence in Subjects With Acne Vulgaris in a Clinic Population Subtitle: Topical Benzoyl Peroxide for Acne
NCT00658112
Analysis of Adherence in Subjects Undergoing Differin Gel, 0.1% Treatment of Moderate to Severe Acne Vulgaris
NCT00696449
Effects of Capsaicin on the Structure, Distribution, and Function of Cutaneous Small Nerve Fibers in Psoriatic Skin
NCT00697034
Expression of Fas Protein in Skin Biopsies of Participants With Scarring Alopecia
NCT00691769
Comprehensive Investigation of Opiates, Neuropeptides, Barrier Function, Scratching and Sleep Physiology
NCT00696397
Benefits of Tanning in Fibromyalgia Patients
NCT00447083
PIE II: Pharmacological Intervention in the Elderly II
NCT00123955
Treatment of Nodular Basal Cell Carcinoma (BCC) With Imiquimod 5% Cream After Curettage
NCT00314756
Thalidomide in the Treatment of Chronic Plaque Psoriasis.
NCT01891019
Cognition in the Study of Tamoxifen and Raloxifene
NCT00687102
Macrolide Antibiotic Therapy for Patients With Cystic Fibrosis
NCT00205634
Women's Health Initiative Study of Cognitive Aging
NCT00631332
Study of Expectorant Activity of Oral N-acetylcystein (NAC) in Patients With Stable Chronic Bronchitis
NCT00205647
Post-hospitalization Nursing Effectiveness (PHONE) Study
NCT00314431
Prospective Aerobic Reconditioning Intervention Study
NCT01113840
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 5 |
| Phase 2 | 10 |
| Phase 3 | 3 |
| Phase 4 | 19 |
Therapeutic Areas
What the Pipeline for Wake Forest University Shows
According to the ClinicalTrials.gov registry, Wake Forest University is linked to 100 US clinical trials across every stage of research activity. Of those, 7 studies are currently recruiting, about 7% of the sponsor's indexed portfolio, and 74 are already marked complete, representing roughly 74% of the total.
The phase mix for Wake Forest University reports 22 late-stage studies (Phase 3 and Phase 4 combined) and 15 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Wake Forest University is Urinary Incontinence with 2 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.