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NCT ID: NCT03956992 Completed - Dental Caries Clinical Trials

Effects of a Hydroxyapatite-based Mouth Gel on Calcium Content of Plaque

Start date: August 8, 2019
Phase: N/A
Study type: Interventional

The aim of this pilot study is to analyze if a hydroxyapatite-containing mouth gel has an influence on the calcium content of plaque.

NCT ID: NCT03948737 Completed - Oxidative Stress Clinical Trials

The Effect of Alpha-tocopherol in Hemolysis and Oxidative Stress Marker on the Red Cell Membrane Beta-thalassemia Major

Start date: December 30, 2016
Phase: N/A
Study type: Interventional

The accumulation of unpaired α-globin chains in β-thalassemia major patients may clinically create ineffective erythropoiesis, hemolysis, and chronic anemia. Multiple blood transfusions and iron overload cause cellular oxidative damage. However, α-tocopherol, an antioxidant, has been known as a potent scavenger of lipid radicals in the red cell membrane of β-thalassemia major patient. By this randomized controlled trial, the investigators would like to evaluate the effects of α-tocopherol in hemolysis and oxidative stress on the red cell membrane of β-thalassemia major.

NCT ID: NCT03946475 Completed - Anemia Clinical Trials

Remaja ASIK and Optimized Food-based Recommendations

Start date: February 8, 2016
Phase: N/A
Study type: Interventional

Good nutritional status among adolescents is a window of opportunity to produce healthy adults or pregnant individuals. Modifying the dietary habits during adolescent girls may be a sustainable approach to ensure good nutritional status among population because those habits tend to stay for a life time. Over many years, there has much effort to overcome anemia. Iron supplementation and fortification have been the most popular and convenient strategies to combat anemia. However, there has not much success due to the high still prevalence of anemia among children and women reproductive age. Food-based approach has been defined as one of the most effective programs to combat or reduce the prevalence of anemia. In the meantime, food based recommendations (FBR) formulation through linear programming (LP) approach has been found to be more effective than the traditional method of developing FBRs called "trial and error". LP approach allows us to develop optimized diet for target population with addition to detect the nutrient problem in specific region. This study therefore aims to identify the nutrient problems in the community, to develop optimized FBR employing the LP approach and to assess effect of nutrition education using optimized FBR in order to improve the nutritional and hemoglobin status among adolescent schoolgirls in rural Malang City. This study was conducted in several phases: 1) cross-sectional study 2) intervention study. Cross-sectional study was aimed to formulate optimized food based recommendations using linear programming. Intervention study was performed during 20 weeks with Remaja ASIK as the tagline which means Active, Healthy, Smart, and Creative. Adolescent schoolgirls aged 14-18 years was the subject of this study and 496 subjects were selected, including 152 for first phase and 344 for third phase. In addition, selected school based on inclusion criteria: 1) not boarding schools; and 2) having large number of students. In doing data collection, we collected socioecodemoghraphic data, anthropometry, biochemical data, dietary data, and cogitive performance.

NCT ID: NCT03945526 Completed - Oxidative Stress Clinical Trials

Effect of Astaxanthin Supplementation on Plasma Malondialdehyde Levels and NIHSS of Stroke Patients

Start date: March 23, 2010
Phase: Phase 1
Study type: Interventional

This is an interventional randomized, controlled trial in analyzing the effects of astaxanthin supplementation on plasma malondialdehyde levels and NIHSS of acute ischemic stroke patients. According to published studies, it was hypothesized that acute ischemic stroke patients who were given astaxanthin would have lower plasma malondialdehyde levels and lower NIHSS score compared to the control group.

NCT ID: NCT03941886 Completed - Pre-Eclampsia Clinical Trials

Implementation of First-trimester Screening and preventiOn of pREeClAmpSia Trial (FORECAST)

FORECAST
Start date: July 31, 2019
Phase: N/A
Study type: Interventional

This implementation study aims to evaluate the efficacy, acceptability, and safety of first-trimester screening and prevention for preterm-preeclampsia. It is a multicenter stepped wedge cluster randomized trial including maternity / diagnostic units from ten regions in Asia. The study involves a period where no intervention will take place at all recruiting units, and then at regular intervals, one cluster will be randomized to transit from non-intervention group to intervention group in which first-trimester screening for preterm-preeclampsia by the Bayes based method followed by the commencement of low-dose aspirin in high-risk women.

NCT ID: NCT03933332 Completed - Clinical trials for Ventilation Therapy; Complications

Correlation Between Muscle Thickness and Inflammation With Ventilator Use in Critically Ill Patients

Start date: October 1, 2018
Phase:
Study type: Observational

Decrease thickness of diaphragm muscle, cross-sectional area of rectus femoris and biceps brachii muscle, and increase in CRP would affect ventilator length of use in critically ill patients in ICU

NCT ID: NCT03933137 Completed - Length of Stay Clinical Trials

P-POSSUM Score and Length of Stay

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

P-POSSUM score had a predictive power of >80% to predict the length of stay of kidney transplant recipients

NCT ID: NCT03930160 Completed - Mortality Clinical Trials

LODS Role in Predicting 30-day Mortality Outcome in ICU

Start date: May 17, 2018
Phase:
Study type: Observational

LODS score for deceased ICU patients within 30 days is higher than survived ICU patients

NCT ID: NCT03930108 Completed - Clinical trials for Mortality Prediction

Validity of SOFA Score as Predictor of Mortality in Critically-ill Burn Patients

Start date: September 17, 2018
Phase:
Study type: Observational

SOFA score is valid for mortality predictor for critically-ill patient in high care and intensive care burn unit

NCT ID: NCT03924076 Completed - Clinical trials for Humoral Immune Response

Effect of Paraprobiotic Lactobacillus Plantarum IS-10506 on Humoral Immune Response of Elementary School Children

Start date: November 14, 2018
Phase: N/A
Study type: Interventional

This study is aimed to determine effect of paraprobiotic Lactobacillus plantarum IS-10506 on humoral immune response by measuring faecal sIgA and blood IgG, IgM, and IgA