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NCT ID: NCT03697304 Active, not recruiting - Neoplasm Metastasis Clinical Trials

Platform Trial Evaluating Safety and Efficacy of BI 754091 Anti- PD-1 Based Combination Therapies in PD-(L)1 naïve and PD- (L)1 Pretreated Patient Populations With Advanced/Metastatic Solid Tumours

Start date: February 12, 2019
Phase: Phase 2
Study type: Interventional

This is a study in adults with various types of advanced cancer. The purpose of the study is to test a medicine called BI 754091 in combination with several other cancer medicines. BI 754091 is an immunotherapy. This means it may help the immune system fight cancer. Such therapies are also called immune checkpoint inhibitors. How long the participants are in the study depends on whether they benefit from treatment and whether they experience unacceptable side effects. The participants are put into different groups. Each group receives BI 754091 in combination with another medicine. The doctors check whether the tumors shrink or disappear. The doctors also check the general health of the participants.

NCT ID: NCT03697096 Active, not recruiting - Clinical trials for Urinary Tract Infection (UTI)

The INSPIRE-ASP UTI Trial

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The INSPIRE-ASP UTI trial is a cluster-randomized controlled trial of HCA hospitals comparing routine empiric antibiotic stewardship practices with real-time precision medicine computerized physician order entry smart prompts providing the probability that a non-critically ill adult admitted with UTI is infected with a resistant pathogen. Note: that enrolled "subjects" represents 59 individual HCA hospitals that have been randomized.

NCT ID: NCT03697070 Active, not recruiting - Pneumonia Clinical Trials

The INSPIRE-ASP PNA Trial

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The INSPIRE-ASP PNA trial is a cluster-randomized controlled trial of HCA hospitals comparing routine empiric antibiotic stewardship practices with real-time precision medicine computerized physician order entry smart prompts providing the probability that a non-critically ill adult admitted with PNA is infected with a resistant pathogen. Note: that enrolled "subjects" represents 59 individual HCA hospitals that have been randomized.

NCT ID: NCT03696953 Active, not recruiting - Clinical trials for Gastrointestinal Symptoms

The Efficacy of Probiotics to Reduce Antepartum Group B Streptococcus Colonization.

Start date: February 1, 2019
Phase: Phase 2
Study type: Interventional

This study is a randomized double blind, placebo controlled trial to determine the efficacy of an oral probiotic in reducing antenatal Group B Streptococcus colonization. The goal of this study is to demonstrate that women in the probiotics group will experience; (1) reduced GBS prenatal colonization at 36± 2 weeks gestation and lower levels of GBS colonization, (2) less need for intrapartum antibiotic prophylaxis and (3) fewer prenatal gastrointestinal symptoms compared to women in the placebo group. Intrapartum measures were added and IRB approved in Feb 2020 as a pilot and feasibility substudy. The goals of this study are as follows: (1) Explore the effect of antepartum exposure to Florajen3 on maternal and neonatal residual GBS and the maternal microbiome. We anticipate that (1)At the time of labor, more women in the probiotics group will test negative for GBS on vaginal to rectal swabs compared to those in the placebo group and (2) Fewer neonates born to women in the probiotic group will have GBS on nasal-oral pharynx cultures within several hours of birth compared to those born to neonates in the control group.

NCT ID: NCT03696797 Active, not recruiting - Diabetes Clinical Trials

Iron Reduction for the Treatment of Diabetes and Nonalcoholic Fatty Liver Disease

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

This is a treatment study to determine if reducing the body's iron stores by blood donation will improve diabetes control and other problems associated with diabetes such as fatty liver disease.

NCT ID: NCT03696277 Active, not recruiting - Clinical trials for Oligoprogressive Renal Cell Carcinoma

SAbR For Oligo-Progressive Renal Cell Cancer.

Start date: October 1, 2018
Phase: Phase 2
Study type: Interventional

Metastatic kidney cancer patients on systemic therapy often develop resistance to limited sites that leads to changing of the systemic therapy. Local therapy to the sites of progression may allow patients to continue on the same systemic therapy that is otherwise effective and being tolerated well. Hypothesis: Stereotactic ablative radiation (SAbR) can delay the change of systemic therapy with oligoprogressive renal cell cancer (RCC) and improve progression free survival (PFS). Primary Objectives: • To evaluate the benefit of SAbR for oligo-progressive mRCC (Metastatic Renal Cell Cancer). Secondary Objectives: • To measure the toxicity, safety and tolerance of concurrent systemic therapy and SAbR for mRCC patients and its impact on quality of life.

NCT ID: NCT03695653 Active, not recruiting - Alcoholism Clinical Trials

Messaging Interventions to Reduce Alcohol Problems Project

MIRAP
Start date: May 24, 2019
Phase: N/A
Study type: Interventional

The study is designed to develop and test a tailored adaptive text messaging/short message service (SMS) intervention for individuals interested in reducing their alcohol consumption. According to the National Institute on Alcohol Abuse and Alcoholism, problem or risky drinking is defined as greater than 7 standard drinks per week for women and 14 standard drinks per week for men. Other groups have other criteria (e.g., 10 drinks for women and 14 for men per week). The Institute of Medicine reports that problem drinkers are those with mild-to-moderate problem severity who do not have physical dependence. Heavy drinking individuals with non-abstinence goals rarely seek treatment for excessive alcohol use, and newer methods such as internet screening and mobile apps provide opportunities to engage and treat this difficult to reach population. There are now 96 mobile phone contracts for every 100 people on earth, making mobile interventions a highly viable method for extending care beyond traditional methods. Text messaging or short message service (SMS) is the most widely available mode of mobile communication and despite its simplicity, has been proven to be a reliable and effective method to induce behavior change across behavioral health targets, including problem drinking. However, large scale randomized controlled trials are needed to provide the necessary empirical evidence to validate SMS interventions and understand the mediators and moderators of outcome for help seeking heavy drinkers who are using or unable to attend in-person care.

NCT ID: NCT03695601 Active, not recruiting - Clinical trials for Heart Transplant Rejection

Surveillance HeartCare® Outcomes Registry

SHORE
Start date: December 28, 2018
Phase:
Study type: Observational

This is an observational registry to assess the clinical utility of surveillance using HeartCare testing services, in association with clinical care of heart transplant recipients.

NCT ID: NCT03695471 Active, not recruiting - Mycosis Fungoides Clinical Trials

Pembrolizumab in Treating Patients With Stage IB-IV Mycosis Fungoides

Start date: December 20, 2018
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well pembrolizumab works in treating patients with stage IB-IV mycosis fungoides. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.

NCT ID: NCT03694600 Active, not recruiting - Liver Cirrhosis Clinical Trials

Clinical Trial Multi-analyte Blood Test

CLiMB
Start date: February 4, 2019
Phase:
Study type: Observational

This is a clinical trial designed to evaluate the performance of a multi-analyte blood test alone to ultrasound alone for the detection of HCC within a population that is at high risk for HCC due to liver cirrhosis.