As of June 2026, 1 paid clinical trial is recruiting for Hidradenitis suppurativa in Bexley, Ohio. Recruiting Hidradenitis suppurativa studies evaluate investigational treatments, diagnostics, and supportive care approaches to improve patient outcomes. Compensation typically covers time, travel, and study visits, and many studies also include study-related medical care at no cost.
Recruiting trial data synced daily from ClinicalTrials.gov. Last sync: .
Bexley has approximately 8 recruiting research studies across a wide range of therapeutic areas. Ohio is home to The Ohio State University Wexner Medical Center, Cleveland Clinic, Cincinnati Children's, and University Hospitals Cleveland Medical Center — collectively running clinical trials across every major therapeutic area.
Researchers run research studies in Bexley, OH at 6 active sites. The clinics below currently host the largest number of recruiting studies — each name is followed by the conditions they focus on most.
| Site | Specializes in | Active trials |
|---|---|---|
| Bexley Dermatology Research | Alopecia, Areata Alopecia, Chronic Spontaneous Urticaria | 2 |
| Investigative | Hidradenitis Suppurativa, Hidradenitis Suppurativa (HS) | 2 |
| Bexley Dermatology (legal entity - Dermatologists of Southwestern Ohio, LLC) | Nonsegmental Vitiligo | 1 |
| Dermatologists of Southwestern Ohio, Llc | NonSegmental Vitiligo | 1 |
| Local Institution - 0177 | Plaque Psoriasis | 1 |
| Oruka Therapeutics Investigative Site | Plaque Psoriasis | 1 |
Clinical trials in Ohio are governed by U.S. Food and Drug Administration (FDA) regulations, Office for Human Research Protections (OHRP) standards, and federal HIPAA privacy rules. Every study is reviewed by an Institutional Review Board (IRB) to protect participant safety and ensure informed consent. Ohio research additionally follows state public health department oversight and any applicable state privacy statutes.
Hipa.ai aggregates every recruiting study in Bexley from ClinicalTrials.gov and refreshes the list daily. Use the filters above to narrow by condition, facility, age, phase, or healthy-volunteer eligibility, then click any study title to view full details — eligibility criteria, intervention, location, and sponsor contact information. To enroll, reach out to the central study contact listed on the study detail page; the research coordinator will walk you through the screening process.
There are approximately 8 recruiting clinical trials in Bexley, Ohio listed on ClinicalTrials.gov. The number changes weekly as new studies open and others close enrollment.
Most recruiting trials in Bexley compensate participants for their time, travel, and study visits. Compensation varies by sponsor, study phase, and visit requirements — the exact amount is disclosed by the study team during the informed consent process.
Eligibility depends on the specific study. Each trial defines its own inclusion criteria (age, diagnosis, medical history, prior treatments) and exclusion criteria. Both patients with specific conditions and healthy volunteers can qualify, depending on the study design.
The most common conditions under active study in Bexley include Plaque Psoriasis (2), Alopecia (1), Areata Alopecia (1), Chronic Spontaneous Urticaria (1), among many others. Browse the list above to explore every recruiting trial.
Yes. Healthy-volunteer studies — often early-phase pharmacology or vaccine trials — recruit in Bexley on an ongoing basis. Use the "Healthy volunteers only" filter above to view trials that accept participants without the study's target condition.
Click any study title above to see the full study record, including eligibility criteria, visit schedule, and the study team's contact information. Reach out to the central contact or recruiting site directly — they will guide you through screening and informed consent.
Recruiting research sites in Bexley include Bexley Dermatology Research, Investigative, Bexley Dermatology (legal entity - Dermatologists of Southwestern Ohio, LLC), among others. Each site lists its open studies and contact information on the study record above — call or email the site coordinator to ask about screening for a specific protocol.