Clinical Trials in Pennsylvania

Showing 10341-10360 of 19,675 trials

Comparison Between iLux and LipiFlow in the Treatment of Meibomian Gland Dysfunction (MGD): A 12-month, Multicenter Study

NCT03956225

The purpose of this post-approval study is to demonstrate that iLux treatment offers comparable treatment effectiveness to LipiFlow for MGD treatment at 12 months post single treatment.

Meibomian Gland DysfunctionEvaporative Dry Eye Disease

Alcon Research299 participantsStarted Jun 2019

Long Beach, California, United States • Los Angeles, California, United States • San Diego, California, United States +12 more locations

TERMINATEDNA86 miles

The (PIVOTAL) Study

NCT00444821

The purpose of this study is to compare endovascular repair using any FDA approved Medtronic AAA Stent Graft System versus surveillance in subjects with smaller abdominal aortic aneurysms (AAA)(4-5CM), with respect to AAA rupture and AAA related deaths.

ABDOMINAL AORTIC ANEURYSMS

Medtronic Cardiovascular728 participantsStarted Mar 2005

Birmingham, Alabama, United States • Tucson, Arizona, United States • Tucson, Arizona, United States +62 more locations

Comparison Between iLux and LipiFlow in the Treatment of Meibomian Gland Dysfunction (MGD): A 12-month, Multicenter Study

The (PIVOTAL) Study

Find Trials by Condition in Pennsylvania

Hydroxychloroquine Monotherapy and in Combination With Azithromycin in Patients With Moderate and Severe COVID-19 Disease

Safety, Tolerability and Efficacy for CGF166 in Patients With Unilateral or Bilateral Severe-to-profound Hearing Loss

Safety, Efficacy and Pharmacokinetics of CF-301 vs. Placebo in Addition to Antibacterial Therapy for Treatment of S. Aureus Bacteremia

A Study of ALKS 3831 in Subjects With Schizophrenia and Alcohol Use Disorder

Phase I/II Study of hLL1-DOX in Relapsed NHL and CLL

Proof of Concept Study Evaluating the Efficacy and Safety of MIJ821 in Patients With Treatment-resistant Depression

Post-market Study to Obtain Surgeon Feedback on Clinical Outcome in Eyes Implanted With TECNIS Toric II IOL

Study of UCART19 in Pediatric Patients With Relapsed/Refractory B Acute Lymphoblastic Leukemia

A Safety Extension Study to Evaluate the Long-term Safety of QGE031 in Chronic Spontaneous Urticaria (CSU) Patients

Long-Term Extension of Previous rAvPAL-PEG Protocols in Subjects With PKU (PAL-003)

Study of Efficacy and Safety of Secukinumab 2 mL Auto-injector (300 mg) in Subjects With Moderate to Severe Plaque Psoriasis

Phase 3 Study Evaluating Safety and Efficacy of OTX-TP in Subjects With OAG or OHT

Manipulating the Microbiome in IBD by Antibiotics and FMT

Study of Efficacy and Safety of LOU064 in Inadequately Controlled Asthma Patients

Study to Assess the Efficacy and Safety of CJM112 in Patients With Inadequately Controlled Severe Asthma

Study of Efficacy of Fevipiprant in Patients With Nasal Polyposis and Asthma

A 12 Week Randomized Open Label Parallel Group Multicenter Study to Evaluate Bioequivalence of 20 mg Subcutaneous Ofatumumab Injected by Pre-filled Syringe or Autoinjector in Adult RMS Patients

Study to Compare QVM149 and Free Triple Combination of Salmeterol/Fluticasone + Tiotropium