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Staten Island, New York Clinical Trials

A listing of Staten Island, New York clinical trials actively recruiting patient volunteers.

RESULTS

Found (15) clinical trials

IBUPAP Study for Pain Management in Children

The investigators' hypothesize the combination of oral ibuprofen and acetaminophen (APAP) is superior to either analgesic alone plus placebo for pediatric emergency department patients with acute mild to moderate traumatic/non-traumatic pain Intent to Treat, prospective, randomized, double-blind trial. Primary outcome: Pain reduction via NRS/FACES pain scale at times 0 and ...

Phase

4.98 miles

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: A Study to Evaluate the Effect of Testosterone Replacement Therapy (TRT) on the Incidence of Major Adverse Cardiovascular Events (MACE) and Efficacy Measures in Hypogonadal Men ( TRAVERSE )

This is a blinded and placebo-controlled study of topical testosterone replacement therapy (TRT) in symptomatic hypogonadal men with increased risk for cardiovascular (CV) disease.

Phase

6.26 miles

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Viveve Geneveve Treatment of the Vaginal Introitus to Evaluate Safety and Efficacy

Decreased sensation and decreased sexual satisfaction following vaginal childbirth has the potential to negatively impact overall sexual function and quality of life in many women. Previous research by obstetricians and gynecologists (OB/GYNs) found that changes in sexual health post-childbirth are not often discussed between physicians and their patients. One possible ...

Phase N/A

7.06 miles

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This study will be evaluating the efficacy, tolerability and safety of an oral medication, Tepilamide Fumarate, compared to placebo in the treatment of moderate to severe plaque psoriasis. This is a phase 3, multi-center, randomized, placebo-controlled, double-blind study with a length of 24 weeks. Visits (9 in-office) can include a ...

Phase

7.3 miles

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This is a double-blind, randomized, placebo-controlled study that evaluates the safety and efficacy of a treatment for correction of moderate to severe cellulite of the buttocks. The study involves at least 5 office visits over the course of the 3 month duration.

Phase

7.3 miles

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This is a double-blind, randomized, placebo-controlled study to assess the efficacy, safety, and tolerability of serlopitant for the treatment of pruritus (itching) in adults with prurigo nodularis (abbreviated as PN, a skin condition with multiple very itchy, solid skin bumps that develop due to scratching).  All enrolled subjects will receive ...

Phase

7.3 miles

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The 12-week, phase 2 study is intended to evaluate the safety and efficacy of IDP-126 Gel, a novel fixed-dose combination of clindamycin phosphate, benzoyl peroxide and adapalene relative to placebo and dual component combinations for the treatment of acne vulgaris in subjects 9 years of age and older. All subjects will ...

Phase

7.3 miles

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This study will be evaluating the efficacy, tolerability and safety of lebrikizumab compared to placebo in subjects with moderate to severe atopic dermatitis. This is a phase 2b, randomized, placebo-controlled, double-blind study in which subjects will be randomized to receive either lebrikizumab 125mg every 4 weeks, 250mg every 2 weeks, ...

Phase

7.3 miles

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This registry aims to characterize the patients who receive DUPIXENT for atopic dermatitis (AD) in a real world setting, with respect to their medical history, socio-demographic and disease characteristics, and prior and concomitant treatments of AD.

Phase

7.3 miles

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The Staying Safe Intervention

HCV infection is the most common chronic blood-borne infection in the U.S., with the overwhelming majority of new HCV infections occurring among people who inject drugs (PWID). Sharing syringes and other injection equipment is the primary risk factor for HCV transmission. HCV prevalence is extremely high in most U.S. PWID ...

Phase N/A

7.96 miles

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