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NCT ID: NCT03120442 Enrolling by invitation - Clinical trials for Postoperative Delirium

Postoperative Delirium After Total Knee Arthroplasty Under Regional Anesthesia

Start date: June 14, 2017
Phase: N/A
Study type: Interventional

Postoperative delirium after total knee replacement surgery has been related to significant morbidity and mortality among high risk patients. Anesthetic care might play a role in the development of postoperative delirium. The purpose of this study is to compare the incidence of postoperative delirium between different intraoperative sedation regimen. Delirium assessment using standardized screening tools will be done every 8 hours after surgery.

NCT ID: NCT03113448 Completed - Clinical trials for Peripheral Diabetic Neuropathy

0.075% Capsaicin Lotion for the Treatment of Painful Diabetic Neuropathy

Start date: January 19, 2017
Phase: Phase 3
Study type: Interventional

To study that 0.075% capsaicin lotion is safe, well tolerated and provide significant pain relief in patients with PDN compared with placebo lotion as a randomized, double- Blind, crossover, placebo-controlled trial

NCT ID: NCT03104829 Recruiting - Diabetes Mellitus Clinical Trials

DSME or DSME + MI in T1DM on Glycemic Control

Start date: October 2016
Phase: N/A
Study type: Interventional

This study evaluates the effect of diabetic knowledge and self care behavior (DSME) alone or DSME plus motivational interviewing on glycemic control among children and adolescents with DM type 1. Half of participants will receive DSME along, while the other half will receive DSME plus MI.

NCT ID: NCT03104673 Completed - Preterm Birth Clinical Trials

Molecular Signature Children

MSP_Ext
Start date: April 30, 2017
Phase:
Study type: Observational

Preterm birth (PTB) occurs before 37 weeks of gestation and is a major cause of neonatal mortality and morbidity. PTB results from heterogeneous influences. One of them is the inherited predisposition of spontaneous PTB, and another is the change in the placental microbial composition as this can cause infections, which lead to inflammation, a common cause of preterm birth. Interestingly, maternal periodontal disease is an independent risk factor for PTB, low birth weight and fetal growth restriction. Immune responses to infectious events or inflammation as well as genetic predisposition to inherited conditions have successfully been studied by using assessing genetic expression profiling. The molecular signature is sets of genes, proteins, genetic variants or other variables that can be used as markers for a particular phenotype. Child morbidity from malnutrition resulting in poor growth and stunting remains a major public health issue that affects the local population just like PTB. While risk factors for malnutrition are multifaceted, there is also a hypothesized causal link between early gut microbiome disruption that leads to chronic malnutrition in otherwise healthy infants. Molecular signatures including the intestinal microbiome development of preterm infants will be evaluated and compared to the term (≥37 weeks' gestation) counterparts. Moreover, a comprehensive examination of possible factors associated with poor growth and poor motor- and neurodevelopment will be assessed. In this extension study: The primary goal for the child is to evaluate the perturbation in the development of the genomic profile including intestinal microbial habitat from children in a rural and limited-resource setting from birth to two years of life.

NCT ID: NCT03103555 Recruiting - Clinical trials for Adult-onset Immunodeficiency

Treatment of Adult-Onset Immunodeficiency With Bortezomib

Start date: February 27, 2017
Phase: Phase 2
Study type: Interventional

This is pilot study aimed to investigate the application of proteosome inhibitor, Bortezomib in treatment of patients with neutralizing autoantibody to IFN-γ. The investigators hypothesis is that bortezomib will reduce the antibody level and restore interferon-gamma function, resulting in clinical improvement and should be well-tolerated and safe for use in patients with autoantibody to IFN-γ.

NCT ID: NCT03098342 Not yet recruiting - Clinical trials for Onychomycosis of Toenail

Comparison of Efficacy and Safety Between Methylene Blue-mediated Photodynamic Therapy and 5% Amorolfine Nail Lacquer for Toenail Onychomycosis Treatment

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

Study centre and address King Chulalongkorn Memorial Hospital Primary objective To compare the efficacy and the safety of methylene blue-mediated photodynamic therapy and 5% amorolfine nail lacquer for toenail onychomycosis in Asians

NCT ID: NCT03098030 Completed - Clinical trials for Small Cell Lung Cancer

Dinutuximab and Irinotecan Versus Irinotecan to Treat Subjects With Relapsed or Refractory Small Cell Lung Cancer

Start date: June 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

This is a 2-part, multicenter, open-label, randomized study of dinutuximab and irinotecan versus irinotecan alone in subjects with relapsed or refractory small cell lung cancer (SCLC). Part 1 of the study involves intrasubject dose escalation to evaluate the safety and tolerability of dinutuximab in combination with irinotecan. Part 2 of the study is designed to determine whether dinutuximab plus irinotecan prolongs overall survival (OS) compared with irinotecan alone. Subjects in Part 2 will be randomized in a 2:2:1 fashion to 1 of 3 treatment groups: (A) irinotecan; (B) dinutuximab plus irinotecan; or (C) topotecan. Randomization will be stratified by duration of response to prior platinum therapy (relapse-free period <3 months or ≥3 months).

NCT ID: NCT03094338 Enrolling by invitation - Clinical trials for Stress, Psychological

A Stress Survey in Nurse Anesthetist Students

Start date: March 1, 2017
Phase: N/A
Study type: Observational

Education is a process of human development for quality of life. Nurse anesthetist students in 1-year training program have to face occasional stress perioperatively such as long and unpredictable working hours, exposure to chemical and radiation hazards, or the occurrence of unexpected death, particularly when a given patient was previously healthy. This can sometimes prove frustrating and may lead to unsafe practices. Students with mild to moderate stress, act as achievement motive, driving them to succeed their goals in learning. However, anyone with severe stress often fails in his or her study. If learners face tension during their education and they are not able to solve it instantaneously; the stress becomes a vicious matter.

NCT ID: NCT03093545 Completed - Rabies Clinical Trials

Effect of Rabies Immunoglobulin on Immunogenicity of Post-exposure Rabies Vaccination in Obese Patients

Start date: March 2015
Phase: N/A
Study type: Interventional

A single center, prospective cohort, open-label study of rabies post exposure program with equine rabies immunoglobulin (ERIG) and purified chick-embryo cell (PCEC) rabies vaccine in WHO category III exposed patients at Siriraj Hospital, Thailand aims to compare serum RVNA responses between obese (BMI > 30 kg/m2) and normal weight/underweight (BMI < 25 kg/m2) and to evaluate adverse events occurring after immunization on days 7, 14 and 28.

NCT ID: NCT03091283 Not yet recruiting - Clinical trials for Educational Problems

Time Management in Nurse Anaesthetist Students

Start date: April 1, 2017
Phase: N/A
Study type: Observational

Nurse anaesthetist student is a registered nurse who spends 1- year training in anaesthesia, has to work laboriously to cope with all assigned activities day and night. Time management, therefore, becomes a practical tool for nurse student to reach her goal. However, many factors act as barriers to nurse students' attaining and maintaining a high grade point average (GPA). Investigators would like to determine the effect of skills in time management on GPA amongst faculty nursing students.