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NCT ID: NCT03524170 Completed - Clinical trials for Anatomic Stage IV Breast Cancer AJCC v8

Radiation Therapy and M7824 in Treating Patients With Metastatic Hormone Receptor Positive, HER2 Negative Breast Cancer

Start date: April 30, 2018
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of anti-PD-L1/TGFbetaRII fusion protein M7824 (M7824) when given together with radiation therapy in treating patients with hormone receptor positive, HER2 negative breast cancer that has spread to other parts of the body. Radiation therapy uses high energy x-rays to kill tumor cells and shrink tumors. M7824 is a drug that targets specific proteins on immune cells in order to activate immune responses against tumor cells. Giving M7824 together with radiation therapy may work better in treating patients with breast cancer.

NCT ID: NCT03523910 Completed - Clinical trials for Pulmonary Arterial Hypertension (PAH)

Right Ventricular Pulmonary Vascular Interaction in Pulmonary Hypertension

Start date: April 25, 2012
Phase: N/A
Study type: Interventional

The goals of this study were two-fold. First, the attempt to quantify the relationships between pulmonary arterial stiffness, right ventricular function and the efficiency of ventricular-vascular interactions in patients with pulmonary arterial hypertension (PAH). Second, the attempt to quantify the effects of exercise on pulmonary arterial stiffness, pulmonary vascular resistance, right ventricular function and the efficiency of ventricular-vascular interactions in patients with PAH.

NCT ID: NCT03523689 Completed - Lung Neoplasm Clinical Trials

Radial-Probe Endobronchial Ultrasound in Detecting Atelectasis in Patients Undergoing Peripheral Bronchoscopy

Start date: April 30, 2018
Phase:
Study type: Observational

This trial studies how well radial-probe endobronchial ultrasound works in detecting the complete or partial collapse of the lung in patients undergoing peripheral bronchoscopy. Diagnostic procedures, such as radial-probe endobronchial ultrasound and bronchoscopy, use a thin, tube-like instrument inserted through the nose or mouth to view and take pictures of the inside of the trachea, air passages, and lungs.

NCT ID: NCT03523624 Completed - Clinical trials for ST-Elevation Myocardial Infarction

Factor XIII and Other Biomarkers in ST Segment Elevation Myocardial Infarction

eXIST
Start date: November 1, 2015
Phase:
Study type: Observational

In medical practice, a combination of clinical exam, electrocardiograms, circulating biomarkers, and imaging is used to gain insights on the prognosis after myocardial infarction. Novel molecular non-invasive tools are needed that help clinicians overcome the adverse events of post-myocardial infarction remodelling and thereby achieve improved therapy for its prevention. Coagulation factor XIII (FXIII) decay has been linked to major adverse cardiac events (MACE) in patients with acute coronary syndromes. Given the correlation between both intramyocardial haemorrhage and microvascular damage with acute phase complications in ST-elevation myocardial infarction, we hypothesise that excessive FXIII decay within the first week may predict acute phase outcomes in these patients. If this holds true, FXIII determination could be used as diagnostic and prognostic tool.

NCT ID: NCT03523598 Completed - Clinical trials for Medicaments Substances in Therapeutic Use

Potassium Nitrate and Post-bleaching Sensitivity

Start date: May 26, 2018
Phase: N/A
Study type: Interventional

This study will determine the effectiveness of the use of desensitivity gels prior in office bleaching on risk and intensity of tooth sensitivity caused by in-office bleaching using 35% hydrogen peroxide and using different types of potassium nitrate. Materials and Methods: Seventy five patients will be selected for this triple-blind, randomized, cross-over, placebo-controlled clinical trial. 10 minutes prior to bleaching procedure, patients will receive the the potassium nitrate 2% or placebo gel application on vestibular surface and Toothpaste 15 days before start the bleaching procedure (group 1: placebo gel + Colgate toothpaste; Group 2: Placebo gel + Nitrate toothpaste Sensodyne and Group 3: Potassium Nitrate + Colgate toothpaste). The whitening treatment with 35% hydrogen peroxide will be carried out in two sessions with a 7-day interval. Tooth sensitivity will be assessed before, during and 24 hours after the procedure using analog visual and verbal scales. Color alteration will be assessed by a Vita Guide scale at the end of the last session. Relative risk to sensitivity will be calculated and adjusted by session; while comparison of overall risk will performed by McNemar's test. Data on the sensitivity level and color shade will be subjected to the Friedman, Wilcoxon (α = 0.05). If necessary, multiple comparation will be done using Tukey's test.

NCT ID: NCT03523481 Completed - Clinical trials for Safety of NHF in Acute Hypercapnic AECOPD

NHF in Acute Hypercapnic Acute Exacerbation of COPD

Start date: May 15, 2018
Phase:
Study type: Observational

Patients with AECOPD and NIV failure and in absence will be treated with NHF device. Inclusion criteria are pH < 7,38 and pCO2 > 45 mm Hg. Patients were treated if pH >7,38 or refusal of therapy.

NCT ID: NCT03523351 Completed - Clinical trials for Metastatic Solid Tumors of Metastatic Disease

Study of Palliative Radiation Therapy vs. no Palliative Radiation Therapy for Patients With High Risk Bone Metastases That Are Not Causing Significant Pain

Start date: May 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to compare the outcome of patients who receive standard treatment versus those who receive preventative radiation and then standard treatment.

NCT ID: NCT03523195 Completed - Sedentary Lifestyle Clinical Trials

Exercise Intervention After Cancer Treatment for Improving Health in Stage II-III Breast Cancer Survivors

PACT
Start date: April 18, 2018
Phase: N/A
Study type: Interventional

This pilot trial studies how well exercise intervention after cancer treatment works in improving physical activity in stage II-III breast cancer survivors. An exercise intervention may promote regular physical activity.

NCT ID: NCT03522948 Completed - Clinical trials for Heavy Drinking and Sexual Risk Behavior

Alcohol and Sex Risk Intervention for MSM Supplement

Start date: November 7, 2017
Phase: N/A
Study type: Interventional

Open pilot trial to test the feasibility and efficacy of a brief intervention with text messaging to reduce sexual risk behavior and heavy drinking among MSM

NCT ID: NCT03522896 Completed - Clinical trials for Effect of Food on Postprandial Hyperglycemia

Effect of Orange Juice on Glycemic Response

Start date: September 30, 2017
Phase: N/A
Study type: Interventional

Orange juice naturally contains high concentrations of hesperidin, which affects glucose absorption in in vitro experiments. This study is to test if hesperidin and other components of orange juice (not other sugars or organic acids) affect the post-prandial blood glucose concentration derived from sugars already present in the orange juice.