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NCT ID: NCT02606019 Recruiting - Dengue Clinical Trials

The Use of Biomarkers in Predicting Dengue Outcome

Start date: October 2015
Phase: N/A
Study type: Observational

The burden of dengue infection has increased due to the current non-specific classification. A pilot study was conducted to evaluate the five of the biomarkers: neopterin, vascular endothelial growth factor (VEGF), thrombomodulin, Vascular Cell Adhesion Molecule 1 (VCAM-1) and pentraxin 3 (PTX-3). VEGF and PTX-3 was the only two potential biomarkers in differentiating severe dengue from non-severe dengue cases. The analysis between severe dengue and non-severe dengue cases indicated that only VEGF was able to discriminate the two categories. Though VCAM-1 and PTX-3 were not statistically significant, the p-values were at the margin of the pre-determined p-value of less than 0.05. Hence, this study aims to evaluate VEGF and PTX-3 levels in differentiating severe dengue from non-severe dengue cases. The secondary objective is to evaluate the correlation of VEGF and PTX-3 levels with full blood count (platelet, white blood cell count and haematocrit) and liver function test (alanine aminotransferase and aspartate).

NCT ID: NCT02578810 Recruiting - Eclampsia Clinical Trials

PIERS and BIS, sFIT:PIGF, Adrenomedullin

BIS2
Start date: October 2016
Phase:
Study type: Observational

Pre-eclampsia, more than being proteinuric gestational hypertension alone, is a state of exaggerated systemic inflammation and remains a leading direct cause of maternal morbidity and mortality worldwide.1 Standardization of antenatal and postnatal assessment and surveillance of pre-eclampsia with protocols that recognize the systemic inflammatory model of preeclampsia have been associated with reduced maternal morbidity.

NCT ID: NCT02541526 Recruiting - Heroin Dependence Clinical Trials

Mirtazapine as a Treatment for Co-Occurring Opioid and ATS Dependence in Malaysia

Start date: May 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate tolerability, acceptability and potential efficacy of 4 months of maintenance treatment with Mirtazapine as compared to placebo for patients with co-occurring amphetamine-type stimulant and opioid dependence (COATS) receiving buprenorphine maintenance treatment (BMT) in Kota Bharu.

NCT ID: NCT02541500 Recruiting - Heroin Dependence Clinical Trials

An Open Label Study of Oral Minocycline for the Treatment of Patients With Co-occurring Opioid and ATS Dependence

Start date: April 2013
Phase: Phase 3
Study type: Interventional

The proposed study will evaluate the tolerability, acceptability and potential efficacy of minocycline for the treatment of co-occurring opioid and amphetamine-type stimulant (ATS) dependence. In the proposed clinical trial, all patients will first discontinue illicit opioid and ATS and be inducted onto buprenorphine maintenance treatment (BMT) in the inpatient ward at the department of psychiatry before beginning to receive minocycline. Tolerability and acceptability will be evaluated by assessing the rates of patient retention during treatment, patient satisfaction with treatment and adverse effects during treatment. The potential efficacy of minocycline will be evaluated with regard to the primary outcome measure: reductions in ATS use , based on urine toxicology testing and self-report. Secondary outcome measures include retention, reduction in HIV risk behaviors and improvements in functional status.

NCT ID: NCT02536079 Recruiting - Brain Injury Clinical Trials

NeuroAiD Safe Treatment Registry

NeST
Start date: June 2014
Phase:
Study type: Observational [Patient Registry]

The NeST registry is a pro-active industry-academic collaboration to assess the use and safety of NeuroAiD in the real world setting. An online entry system was set up to allow easy data entry and retrieval of clinical information.

NCT ID: NCT02523846 Recruiting - Post-operative Pain Clinical Trials

Patient Re-education vs. Background Morphine to IV-PCA in Patient With Unsatisfactory Analgesia Post Laparotomy

Start date: August 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to improve IV-Patient Controlled Analgesia (IV-PCA) technique for postoperative analgesia. Investigators are comparing between patient re-education and the background morphine infusion among patients who fail to achieve satisfactory analgesia using IV-PCA Morphine after laparotomy.

NCT ID: NCT02510131 Recruiting - Clinical trials for Urinary Incontinence

Is Hyacinth Exercise Better Than Kegel's Exercise in Women With Urinary Incontinence?

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

To determine whether Hyacinth exercises are more effective than Kegel's exercise at improving pelvic floor weakness among women aged 55 and above with urinary incontinence.

NCT ID: NCT02498119 Recruiting - Clinical trials for Type 2 Diabetes Mellitus

The Role of Arachidonic Acid Metabolites, From Patients With Metabolic Syndrome

Start date: November 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to determine whether an increase in lipid bodies in leukocytes will lead to an increase in eicosanoid production. The 2nd purpose is to determine if there is a significant correlation between lipid body formation and enhanced generation of both Lipoxygenase (LO) and COX derived eicosanoids. The 3rd purpose is, if lipid bodies are involved in arachidonic acid (AA) metabolism, then AA present in these lipid rich structure must be released by phospholipases and the free Arachidonic Acid (AA) must have access to the eicosanoid forming enzyme. The fourth objective is to determine the compartmentalisation of cPLA2 and MAP kinases including ERK1, ERK2, p85 and p38 are involved in AA liberation within lipid bodies.

NCT ID: NCT02492087 Recruiting - Clinical trials for Postpartum Haemorrhage

Topical Tranexamic Acid in Caesarean Section

TXACS
Start date: August 2015
Phase: Phase 3
Study type: Interventional

The objective of this study is to investigate whether topical application of tranexamic acid into the uterine cavity and the surgical site intra-operatively can reduce blood loss and provide better surgical haemostasis in parturients with moderate to high risk for bleeding undergoing caesarean deliveries.

NCT ID: NCT02479113 Recruiting - Clinical trials for Metabolic Syndrome X

Maternal Hypertriglyceridaemia Study

Start date: March 2014
Phase: N/A
Study type: Observational

Besides maternal hyperglycemia, a strong link between maternal pregravid weight/maternal triglyceride(Tg) levels and fetal growth/childhood obesity/metabolic syndrome in offspring has been demonstrated in largely Caucasian populations. This study aims to explore the link between maternal hypertriglyceridemia and offspring health in Asians.