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Adverse Reaction to Drug clinical trials

View clinical trials related to Adverse Reaction to Drug.

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NCT ID: NCT01830257 Enrolling by invitation - Clinical trials for Adverse Reaction to Drug

Explore Active Surveillance Mode of the Community's Adverse Event Following Immunization(AEFI)

AEFI
Start date: April 2013
Phase: Phase 4
Study type: Interventional

The investigators would remind the guardians of observation after immunization via sending short message and collect the information of AEFI by two ways, short message/telephone and website questionnaire.

NCT ID: NCT01621373 Completed - Clinical trials for Adverse Reaction to Drug

Exploratory Propofol Dose Finding Study In Neonates

NEOPROP
Start date: August 2012
Phase: Phase 2
Study type: Interventional

The aim of the study is to explore the optimal propofol dose in neonates receiving a single intravenous propofol bolus for endotracheal intubation during (semi-)elective INSURE (intubation-surfactant-extubation) procedure (preterm neonates) and (semi-)elective non-INSURE procedures (term-preterm neonates).

NCT ID: NCT01600677 Terminated - Clinical trials for Medication Adherence

Determining the Impact of a Medication Delivery Unit on Medication Adherence of Adults With Common Cardiac Conditions

EMMA-RCT
Start date: May 2012
Phase: N/A
Study type: Interventional

The research study is a randomized controlled trial (RCT). The primary endpoint is to compare medication adherence of adult patients recently hospitalized with a diagnosis of common cardiac conditions who require medication assistance either by receiving usual care or by using a medication delivery unit. The overall study will last a total of 12 months. Each subject will be enrolled for a period of 90 days.

NCT ID: NCT01430702 Withdrawn - Clinical trials for Medication Adherence

Feasibility of Using a Telemedicine Medication Delivery Unit for Older Adults

EMMA
Start date: September 2011
Phase: N/A
Study type: Interventional

Care transition interventions have been successful in reducing medication-related problems and associated rehospitalization primarily by focusing on medication reconciliation conducted by trained healthcare professionals. Programs to improve the medication reconciliation process have largely been effective, but have limitations including the expense associated with recruiting, training, and retaining care transition healthcare professionals (e.g., nurses and nurse practitioners) the ability to provide services within a finite geographic area, and the retrospective nature of the reconciliation process which usually occurs in the home following hospital discharge. Our short-term objective is to use Pennsylvania Department of Aging resources to assess the feasibility of using a telemedicine medication delivery unit for frail older adults that require medication assistance in their home immediately following an acute hospitalization. As part of this feasibility assessment, the investigators will assess (1) recruitment process and procedures, (2) data collection procedures, (3) resource utilization, (4) drop-out rates, (5) acceptability and usability of the EMMA® telemedicine medication delivery unit, (6) medication adherence, and (7) medication-reconciliation errors during transition from hospital to home.

NCT ID: NCT01354197 Recruiting - Critical Illness Clinical Trials

The Thai Surgical Intensive Care Study (Thai-SICU Study)

THAI-SICU
Start date: April 2011
Phase: N/A
Study type: Observational

- Overall treatment outcomes of University base SICU - Incidence of adverse events in SICU - Factor associated to adverse events in SICU

NCT ID: NCT01237275 Active, not recruiting - Depression Clinical Trials

Development of A Technique to Predict Antidepressant Responsiveness in Depressive Patients

Start date: October 1999
Phase: N/A
Study type: Interventional

First, the investigators examined the functional relevance of serotonin transporter polymorphisms by quantifying the activity of serotonin transporter in blood platelets of genotyped healthy volunteers and patients with major depression. Second, the investigators studied response to SSRIs in relation to 5-HTTLPR genotype and also to the functional expression of 5-HTT in platelets.

NCT ID: NCT00935246 Active, not recruiting - Depression Clinical Trials

Development of Escitalopram Genomic Device by Using Candidate Gene Approach and Genome-Wide Scanning

Start date: December 2008
Phase: N/A
Study type: Interventional

To reveal the genetic determinants of the treatment outcome of escitalopram in depressed patients (by using candidate gene approach and whole genome scanning).

NCT ID: NCT00817375 Recruiting - Depression Clinical Trials

Pharmacogenomic Study to Predict Antidepressant Responsiveness in Depressed Patients

Start date: February 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether pharmacogenomic study predict antidepressant responsiveness in advance before the appearance of the drug effects until 4~6 weeks after drug administration.