Ulcerative Colitis Clinical Trials in Chicago

Showing 361-380 of 806 trials

Expanded Access Program for Idebenone in Participants With Duchenne Muscular Dystrophy (DMD)

NCT03433807

The primary objective of this Expanded Access Program is to provide idebenone as a treatment for eligible participants with Duchenne Muscular Dystrophy before it is commercially available in the United States (U.S.) for the indication of DMD.

Duchenne Muscular Dystrophy

Santhera Pharmaceuticals

Phoenix, Arizona, United States • New Haven, Connecticut, United States • Chicago, Illinois, United States +9 more locations

COMPLETEDNA2.2 miles

Early Amniotomy Versus Delayed Amniotomy Following Foley Catheter Ripening in Nulliparous Labor Induction

NCT03039036

Amniotomy (breaking the bag of water) is commonly used in the induction of labor. However, the timing is highly variable. The purpose of this study is to determine if first time mothers undergoing induction of labor with a Foley catheter experience a decrease in their labor time when undergoing early amniotomy (breaking the bag of water within 1 hour of Foley catheter removal) than when undergoing delayed amniotomy (breaking the bag of water at least 4 hours after Foley catheter removal). Other aims include the relationship between timing of amniotomy and cesarean section, postpartum hemorrhage, intrauterine infection, neonatal Apgar score \<7 at 5 minutes, neonatal need for intensive care. The investigators hypothesize that induction of labor with Foley catheters followed by early amniotomy will result in a decreased duration of labor compared to those who undergo delayed amniotomy.

Labor Induction

Northwestern University69 participantsStarted Sep 2017

Chicago, Illinois, United States

Expanded Access Program for Idebenone in Participants With Duchenne Muscular Dystrophy (DMD)

Early Amniotomy Versus Delayed Amniotomy Following Foley Catheter Ripening in Nulliparous Labor Induction

Ulcerative Colitis Trials in Other Cities

S1316, Surgery or Non-Surgical Management in Treating Patients With Intra-Abdominal Cancer and Bowel Obstruction

Transdermal or Oral Telapristone Acetate in Treating Patients Undergoing Mastectomy

Respiratory Infection Monitoring

Etrasimod Versus Placebo for the Treatment of Moderately to Severely Active Ulcerative Colitis

Multicenter Investigation of Trabecular Micro-Bypass Stents vs. Laser Trabeculoplasty

A Randomized, Double Blind, Placebo Controlled Study of Etanercept in Children With Kawasaki Disease

Study to Assess the Effect of Omecamtiv Mecarbil on Exercise Capacity in Subjects With Heart Failure

Ipilimumab and Nivolumab as Adjuvant Treatment of Mucosal Melanoma

Multi-Center Trial Utilizing Low Frequency Ultrasound in the Prevention of Post-Contrast Acute Kidney Injury

FX-322 in Adults With Stable Sensorineural Hearing Loss

A Phase 1 Open-Label, Dose Escalation Study to Determine the Optimal Dose, Safety, and Activity of AAV2hAQP1 in Subjects With Radiation-Induced Parotid Gland Hypofunction and Xerostomia

Two-Part Dose-Confirming Study of Pulsed Inhaled Nitric Oxide in Subjects With WHO Group 3 Pulmonary Hypertension Associated With COPD

Safety, Tolerability, and Pharmacokinetics of Oral NX-13 in Active Ulcerative Colitis

Improving Quality by Maintaining Accurate Problems in the EHR

The CAPTURE Study: Validating a Unique COPD Case Finding Tool in Primary Care (Aim 2)

First-in-human Study of BAY2287411 Injection, a Thorium-227 Labeled Antibody-chelator Conjugate, in Patients With Tumors Known to Express Mesothelin

A Phase I Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of CT-G20 in Subjects With Obstructive Hypertrophic Cardiomyopathy

International CoolSculpting: Study to Evaluate Patient Satisfaction for Non-Invasive Fat Reduction in Abdomen and/or Flanks (iCOOL)

Other Conditions in Chicago