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A, Concord N Clinical Trials

A listing of A, Concord N clinical trials actively recruiting patients volunteers.

RESULTS

Found (738) clinical trials

Having trouble going to the bathroom? Don’t be embarrassed — explore your options. Researchers are gathering additional information about the effectiveness of an investigational product for treating irritable bowel syndrome with constipation (IBS-C).

Phase N/A

A Randomized, Double-Blind, Placebo-Controlled, Phase 2B Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of ASN002 in Subjects With Moderate to Severe Atopic Dermatitis

Phase

ICON Early Phase Services is conducting a research study for healthy adults ages 21-65. This is a device study testing for the level of blood alcohol after the consumption of liquor.    Vital signs, ECGs, physical examinations and pregnancy, drug and alcohol screens will be performed. Blood and urine samples ...

Phase

Primary end point: To evaluate the safety and tolerability of INCB054707. Secondary end point: To evaluate the systemic exposure and evaluate the efficacy of INCB054707. Overall design: This is a Phase 2, multicenter, open-label, single-arm study to assess the safety of 15 mg QD INCB054707 over 8 weeks in men and women aged 18 ...

Phase

The purpose of this research study is to collect information on the safety of the TactiCath SE ablation catheter when it is used to treat atrial fibrillation in people like you. This study will collect information about the success of the procedure and report on the number and type of ...

Phase N/A

Preeclampsia is a complication of pregnancy. Preeclampsia may occur from 20 weeks’ pregnancy through the delivery and postpartum period.  Preeclampsia does not occur in every pregnant woman. It is thought that preeclampsia occurs in about 3 to 5 out of a total of 100 pregnant women. A higher number of ...

Phase N/A

Bothered by Rosacea on Your Face? Join a clinical research study of the safety and effectiveness of an investigational spray for people with mild to moderate rosacea. Participants will use the product twice a day for eight weeks.

Phase N/A

The purpose of the RADIANCE-HTN study is to demonstrate the ability of the Paradise System to effectively reduce systolic daytime ambulatory BP (ABP) in hypertensive subjects. In addition the study is designed to document the safety profile of the Paradise System in all treated subjects.

Phase N/A

The primary objective is to understand the role of ATP in primary prevention patients indicated for ICD therapy. The incidence of all-cause shocks in subjects programmed with shocks only will be compared with subjects programmed to standard therapy (ATP and shock) to assess equivalency. Multivariate analyses will also be performed to ...

Phase N/A

The purpose of this post-market feasibility study is to evaluate whether DyeVert Plus Contrast Reduction System use during standard angiography procedures involving the use of OCT result in contrast media (CM) volume savings without reducing image quality. The primary objective of this study is to evaluate the volume (percentage) of ...

Phase N/A