Clinical Trials Logo

Filter by:
NCT ID: NCT02135770 Completed - Clinical trials for Severe Sepsis With Septic Shock

Impact of Low Dose Unfractionated Heparin Treatment on Inflammation in Sepsis

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

Sepsis is a clinical syndrome which infection trigger systemic inflammatory response. Uncontrolled inflammatory process leads to multiple organ dysfunction and cause early mortality in severe sepsis. Unfractionated heparin is an anticoagulant that widely used either for DVT prophylaxis or treatment of disseminated intravascular coagulation. Heparin also have an anti-inflammatory effect through downregulates nuclear factor kappa B and tumor necrosis factor alpha. Aim of this study is to determine effects of low dose unfractionated heparin treatment on inflammation in severe sepsis patient.

NCT ID: NCT02121314 Completed - Tuberculosis Clinical Trials

HRZE Fasted/Fed in Newly Diagnosed TB

FASTFOOD
Start date: July 2013
Phase: Phase 2
Study type: Interventional

WHO recommends to take TB drugs while fasting: if TB drugs are taken with food, perhaps drug concentrations are too low; on the other hand: if this is not tolerated, drugs could also be taken with food. Do lower drug concentrations - with improved adherence to therapy - outweigh the disadvantage of lower drug blood concentrations over time? How exactly do the drug concentrations over time (pharmacokinetics) compare between fasting and fed conditions, especially in the early stage of TB treatment when patients are relatively sick, and relatively poorly tolerate TB drugs?

NCT ID: NCT02106039 Completed - Diabetes Mellitus Clinical Trials

Pulmonary Tuberculosis Patients With Diabetes Mellitus

TANDEM
Start date: April 28, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of enhanced glycemic monitoring of diabetes upon diabetes glycaemic control during tuberculosis treatment in tuberculosis- diabetes patients.

NCT ID: NCT02105714 Completed - Schistosomiasis Clinical Trials

Diagnosis of Neglected Tropical Diseases Among Patients With Persistent Digestive Disorders

NIDIAGDigest
Start date: July 2014
Phase: N/A
Study type: Observational

NIDIAG is an international collaboration on integrated diagnosis-treatment platforms, funded by the European Commission (EC). NIDIAG aims to develop an improved, patient-centred system for delivering primary health care in resource-constrained settings. NIDIAG will investigate three clinical syndromes, namely (i) persistent digestive disorders, (ii) persistent fever and (iii) neurological disorders, due to neglected tropical diseases (NTDs). The current study focuses on persistent digestive disorders, which are defined as diarrhoea or abdominal pain that last for at least 2 weeks. While acute diarrhoea has been studied globally, few research activities have focused on the epidemiology, diagnosis and treatment of long-lasting diarrhoeal episodes (2 weeks and longer) in the tropics. The spectrum of possibly involved pathogens includes more than 30 bacterial, parasitic and viral infectious agents. This lack of data may be explained by the fact that people suffering from NTDs might only seek care at a late stage of the disease. Furthermore, health systems in affected regions are often weak and their primary health-care centres are often under-staffed and lack essential diagnostic equipment. The hypothesis of this study is that development of an evidence-based syndromic approach can lead to better diagnosis and management of NTDs in patients with persistent digestive disorders. The study will be carried out in two West African countries (Côte d'Ivoire and Mali) and in two Asian countries (Indonesia and Nepal). The study will follow a "case-control" design and patients and controls will be prospectively enrolled. In order to address the knowledge gaps, three specific objectives will be pursued. First, the contribution of NTDs to the 'persistent digestive disorders syndrome' will be assessed. Second, the value of clinical features and rapid diagnostic tests (RDTs) for the diagnosis of target NTDs that give rise to persistent digestive disorders will be determined. Third, the clinical response to standard empiric and targeted treatment of several NTDs in patients with persistent digestive disorders will be evaluated. These objectives will provide a long-term benefit for the communities by improving the clinical decision-making process for the target NTDs and thus, better diagnostic work-up and patient management can be achieved in the study countries and other similar resource-constrained countries

NCT ID: NCT02105493 Completed - Clinical trials for Injury of Radial Artery

Nitroglycerin Prevents Radial Artery Occlusion

NORAO
Start date: October 2013
Phase: N/A
Study type: Interventional

Trans-radial approach (TRA) has becoming popular and widely adopted over the last decade. However, radial artery occlusion (RAO) continues to be one of the limitation of trans-radial access and potentially limits the radial artery as an access site in the future. Several strategies have been used to decrease the incidence of RAO including the use of anticoagulation, maintenance of patency during hemostasis, or shortening the duration of compression. Currently, there is no data whether vasoactive pharmacological therapy such as nitroglycerin administered intra-arterially at the end of the procedure may reduce the incidence of RAO. It is hypothesized that the addition of nitroglycerin (nitric oxide donor) at the end of a TRA procedure may reduce the incidence of RAO.

NCT ID: NCT02104518 Completed - Clinical trials for Glucose-6-Phosphate Dehydrogenase Deficiency

Evaluation of Different G6PD Testing Platforms

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

In this study the investigators propose to evaluate the performance of several G6PD testing platforms.

NCT ID: NCT02095314 Completed - Healthy Clinical Trials

Antibody Persistence, Immune Response and Safety After Doses of Pentabio Vaccine

Start date: March 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Measure antibody persistence prior to booster administration of Pentabio vaccine.

NCT ID: NCT02093286 Completed - Healthy Clinical Trials

Safety Profile Following Pentabio Vaccination in Indonesian Infants

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

To assess any serious systemic reaction within 30 minutes after Pentabio immunization

NCT ID: NCT02093273 Completed - Healthy Clinical Trials

Evaluation on Immunogenicity and Safety Profile of Trivalent OPV (tOPV Bio Farma)

Start date: May 2013
Phase: Phase 2
Study type: Interventional

The objective of this study is to compare the antibody response 30 days after two doses of t OPV

NCT ID: NCT02093260 Completed - Healthy Clinical Trials

Immunogenocity and Safety of Flubio (Influenza HA) Vaccine in Infants and Children (Bridging Study)

Start date: May 2014
Phase: Phase 2/Phase 3
Study type: Interventional

To Asses the Immunogenicity and Safety of Flubio (Influenza HA) Vaccine in Infants and Children (Bridging Study)