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NCT ID: NCT03596866 Active, not recruiting - ALK+ Advanced NSCLC Clinical Trials

A Study of Brigatinib Compared to Alectinib in Adults With Non-Small-Cell Lung Cancer

ALTA-3
Start date: April 19, 2019
Phase: Phase 3
Study type: Interventional

Brigatinib is a medicine that binds to the surface of tumor cells in some cancers and delivers a dose of chemotherapy directly to the tumor. In this study, participants will be people with non-small-cell lung cancer (NSCLC for short). The main aim of the study is to learn if brigatinib stops the tumors from growing, or if the tumors have shrunk or disappeared, compared to a medicine called alectinib. At the first visit, the study doctor will check who can take part. Participants who can take part will be picked for 1 of 2 treatments by chance: - Brigatinib tablets - Alectinib capsules All participants will take brigatinib or alectinib at about the same time every day. They will continue with treatment throughout the study unless their cancer gets worse, they have side effects from the treatment, they leave the study for certain reasons, or the study is stopped. After stopping treatment, participants will visit the study clinic for a check-up 30 days later.

NCT ID: NCT03596736 Completed - Clinical trials for Distal Humerus Fracture

Elbow Hemiarthroplasty Versus Total Elbow Arthroplasty for Irreparable Distal Humeral Fractures

Start date: January 19, 2011
Phase: N/A
Study type: Interventional

Distal humeral fractures can be difficult to treat, in particular when the joint surface is affected (intra-articular fractures). If rigid internal fixation with plates and screws can be obtained it is considered to be the treatment of choice. In elderly patients, poor bone quality (osteopenia) and fragmentation of the articular surface can make rigid internal fixation non-reliable or even impossible. Total elbow arthroplasty has been shown to be of value in this type of situation. Elbow hemiarthroplasty has been proposed as an alternative to total elbow arthroplasty. The theoretical advantages as opposed to total elbow arthroplasty are: no restriction in the weight allowed to be lifted, complications related to polyethylene wear debris are avoided as there is no polyethylene liner and there is no ulna component that can loosen. Wear of the native ulna and instability are potential complications of elbow hemiarthroplasty. The aim of this multicenter study is to test the hypothesis that elbow hemiarthroplasty gives better elbow function than total elbow arthroplasty for irreparable distal humeral fractures.

NCT ID: NCT03596255 Completed - Dental Anxiety Clinical Trials

Clinical Estimation of Dental Anxiety

Start date: September 1, 2017
Phase:
Study type: Observational

Introduction: Dental anxiety (DA) is treatable and preventable when dental personnel correctly estimate the patient's level of DA. Objective: To evaluate dental personnel's ability to estimate DA.

NCT ID: NCT03593382 Completed - Clinical trials for Female Athlete Triad

Energy Availability in Female Athletes

Start date: November 2011
Phase:
Study type: Observational

The purpose of this project is to study the impact of energy availability (EA) on female endurance athletes and the adaptive consequences of insufficient EA with a special reference to the impact on energy metabolism, reproductive-, vascular- and bone health as well as exercise capacity, neuromuscular performance, ability to recover from intense exercise and the genetic interaction. Specific aims: - To investigate the effects of EA on energy metabolism - To investigate the effects of EA on reproductive, vascular- and bone health, and endocrine functions - To investigate the effects of EA on exercise capacity - To investigate the effects of EA on neuromuscular performance - To investigate the effects of EA on recovery after exercise - To identify potential dietary factors influencing EA, exercise capacity and neuromuscular performance - To identify potential exercise factors influencing EA, exercise capacity and neuromuscular performance - To identify potential psychological, behavoural and motivational aspects associated with insufficient EA The investigators hypothesize that female athletes with insufficient energy availability have attenuated energy metabolism, reduced BMD, impaired endothelial function and decreased ability to recover between exercise bouts compared to matched controls with sufficient energy and nutrient intake. The investigators also hypothesize that EA influences exercise capacity and neuromuscular performance.

NCT ID: NCT03590405 Completed - Infertility, Female Clinical Trials

Uterus Transplantation LD - Feasibility Study - Sahlgrenska - BMC

GOT-BMC-UTx
Start date: June 15, 2018
Phase: N/A
Study type: Interventional

Medical know-how concerning uterus transplantation will be transferred to new site by structured process involving theory, animal workshops and a clinical feasibility study on human subjects.

NCT ID: NCT03590171 Recruiting - Clinical trials for Acute Lymphoblastic Leukemia (ALL)

International Study for Treatment of High Risk Childhood Relapsed ALL 2010

Start date: September 1, 2017
Phase: Phase 2
Study type: Interventional

The main goal of this study is to improve the outcome of children and adolescents with acute lymphoblastic leukemia with high risk first relapse by optimization of treatment strategies within a large international trial and the integration of new agents.

NCT ID: NCT03587376 Completed - Alzheimer Disease Clinical Trials

Characterization of T-Cell Response in Participants Previously Treated With JNJ-54861911 (Atabecestat)

Start date: May 30, 2018
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to determine T-cell mediated inflammatory immune response in some participants previously exposed to atabecestat.

NCT ID: NCT03587116 Active, not recruiting - Hemophilia A Clinical Trials

A Study to Evaluate Prospective Efficacy and Safety Data of Current FIX Prophylaxis Replacement Therapy in Adult Hemophilia B Subjects (FIX:C≤2%) or Current FVIII Prophylaxis Replacement Therapy in Adult Hemophilia A Subjects (FVIII:C≤1%)

Start date: July 26, 2018
Phase: Phase 3
Study type: Interventional

To establish baseline prospective efficacy data of current FIX prophylaxis replacement therapy in the usual care setting of hemophilia B subjects, who are negative for nAb to AAV-Spark100, prior to the Phase 3 gene therapy study. To establish baseline prospective efficacy data of current FVIII prophylaxis replacement therapy in the usual care setting of hemophilia A subjects, who are negative for nAb to AAV6, prior to the Phase 3 gene therapy study. The enrollment for hemophilia A participants is completed. At this time participants are only being enrolled for hemophilia B cohort.

NCT ID: NCT03586856 Completed - Infant,Premature Clinical Trials

Comparison of Leakage With Nasal Prongs and Nasal Mask Interface in Newborns Receiving CPAP Treatment

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

The study is a two-armed randomized cross-over comparison of leakage with nasal prongs and nasal mask interface in newborn infants treated with CPAP, born after 28 weeks of gestational age. For infants with an interface leakage, the trial also includes an observational part evaluating simple measures to reduce leakage. The study will be carried out in the Karolinska University Hospital Stockholm and in the Östersund Hospital.

NCT ID: NCT03586011 Completed - Physical Activity Clinical Trials

Predictors of Increased Physical Activity in Patients Receiving Physical Activity on Prescription

Start date: January 1, 2010
Phase:
Study type: Observational [Patient Registry]

The aim of this study is to explore possible predicting factors associated with physical activity (PA) level change in a 6-month period of physical activity on prescription (PAP) treatment. This is done in order to highlight potential predictors important for increased PA-level and to identify which primary care patients who may benefit from the PAP-intervention. Four hundred forty four patients are included in the study, 27-85 years, physically inactive, having at least one component of the metabolic syndrome (MetS) present and receiving PAP-treatment. Possible predicting factors of PA change at baseline and PA-level at 6-month follow-up are analyzed.