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Emergencies clinical trials

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NCT ID: NCT00573599 Completed - Clinical trials for Acute Migraine Headache

Prochlorperazine vs Imitrex for Acute Migraine in the Emergency Department

Start date: February 2007
Phase: N/A
Study type: Interventional

ED patients with acute migraine will be randomized to either prochlorperazine and Bendaryl OR imitrex. VAS for pain will be monitored, along with side effects. Primary outcome measure is improvement in pain scales between the groups.

NCT ID: NCT00548041 Completed - HIV Infections Clinical Trials

Rapid HIV Testing Program in the Emergency Department

Start date: April 2007
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the feasibility of a rapid HIV testing program in the Temple University Hospital(TUH)Emergency Department. We hypothesize that a rapid HIV testing program in the TUH Emergency Department is feasible. Patients presenting to the Adult TUH Emergency Department with certain conditions will be offered rapid HIV testing. Testing will be performed by oral swab using the OraQuick Advance test. Patients will receive post-test counseling.

NCT ID: NCT00510783 Completed - Clinical trials for Tonic-clonic Seizure

IV Keppra in the Emergency Department for Prevention of Early Recurrent Seizures

Start date: July 2007
Phase: Phase 4
Study type: Interventional

This study is looking at three seizure medicines. Patients with seizures are usually treated with phenytoin (Dilantin) or Fosphenytoin. These medicines can be given intravenously (IV)or by mouth. Another seizure medicine, levetiracetam (Keppra) can now be given this way also. This study will compare IV phenytoin (Dilantin) and IV fosphenytoin to levetiracetam (Keppra) in patients who have had a recent seizure. Only patients with a history of seizures can be involved. The patient must present to the emergency department within 4 hours of a seizure. The purpose of this study is to compare these three drugs, phenytoin (Dilantin), fosphenytoin, and levetiracetam (Keppra). The investigators are looking to see if these drugs can prevent another seizure in the next 24 hours. We are also looking for any possible side effects.

NCT ID: NCT00504283 Completed - Kidney Stone Clinical Trials

An Analgesia Protocol for Acute Renal Colic in the Emergency Department

Start date: February 2007
Phase: N/A
Study type: Interventional

An analgesia protocol for acute renal colic will lead to faster significant reductions in pain than prior practice.

NCT ID: NCT00497393 Completed - Acute Illness Clinical Trials

Clinical Decision Unit (CDU) - Evaluation of a Novel Approach to Address Emergency Department Overcrowding

Start date: July 2007
Phase: Phase 4
Study type: Interventional

This randomized controlled trial will introduce a Clinical Decision Unit (CDU) into the University of Alberta Hospital Emergency Department(ED)and assess the influence on ED length of stay, patients who leave without being seen, and other ED Overcrowding outcomes.

NCT ID: NCT00457600 Completed - Asthma Clinical Trials

ParentLink: Better and Safer Emergency Care for Children

Start date: June 2005
Phase: Phase 2/Phase 3
Study type: Observational

The emergency department (ED) constitutes a high-risk environment for errors and poor quality of care. Pediatric patients are at increased risk of medical errors. We postulate that implementation of a patient-centered health information technology - ParentLink - can address system-level deficiencies and the unique “just-in-time” information needs of ED physicians and the parents of ill children. The proposed work delivers an innovative product – an electronic interface linked to a pediatric knowledge base that integrates parent-derived data with best practices for safe and effective emergency care across common pediatric disease conditions: otitis media, urinary tract infections, asthma, and head trauma. The study has two aims, the first of which addresses critical gaps in data capture: to evaluate the completeness and accuracy of information on symptoms, disease condition, medications and allergies generated by parents using ParentLink versus information documented by ED physicians and nurses, using structured telephone interviews as a gold standard. The second aim measures the ParentLink’s impact on ED patient safety and quality, specifically: a) the error rate for ordering and prescribing of medications during ED care, and b) the percent of ED visits that adhere to national evidence-based guidelines. Parentlink will be rigorously evaluated in a clinical trial at two diverse ED sites and will use a sequential, non-randomized observational design with two intervention and two control periods to measure the effects of ParentLink on data capture and safety and quality of patient care.

NCT ID: NCT00457366 Completed - Agitation Clinical Trials

A Comparison Study of the Efficacy of Quetiapine and Haloperidol in Agitated Adults in Emergency Room

Start date: May 2006
Phase: Phase 4
Study type: Interventional

In the Psychiatric Emergency Room, agitated patients are treated routinely with an I.M. Haloperidol "cocktail" (Haloperidol 5 mg, Lorazepam 2 mg, Cogentin 2 mg), which has proved to be an effective treatment. However, since it is an intramuscular injection, it is more complicated and perhaps less acceptable to patients as well as more likely to cause EPS (extrapyramidal symptoms). Of late in our emergency room, we started using high dose Quetiapine 300 mg PO to replace the "cocktail" for treating agitation. It has shown promising results.

NCT ID: NCT00456391 Completed - Convulsions Clinical Trials

The Utility of Performing Brain CT Scan in Non Trauma Patients at the Pediatric Emergency Unit

Start date: October 2006
Phase: N/A
Study type: Observational

Pediatric patients are admitted to the emergency room for diverse causes, beside trauma, patients can present with convulsions, suspicion of brain tumor or increased intracranial pressure. In most of the cases a brain CT is performed even before physical examination by a skilled neurologist. The amount of radiation that the children are exposed is equivalent to 100 plain chest X rays. The purpose of this tudy is to examinate in a retrospective study what were the indications for CT study and what was the incidence of relevant abnormal findings that required emergency intervention or referral.

NCT ID: NCT00449787 Completed - Migraine Clinical Trials

Comparing Naproxen to Sumatriptan for Emergency Headache Patients

HEDNet2
Start date: March 2007
Phase: Phase 4
Study type: Interventional

2/3 of patients discharged from an emergency department after treatment for an acute headache will still be bothered by headache within 24 hours of emergency department (ED) treatment. The goal of this study is to compare two medications, naproxen and sumatriptan, to determine which is better for the treatment of recurrent headache within 24 hours of emergency department discharge.

NCT ID: NCT00448331 Completed - Mental Disorders Clinical Trials

Facilitated Referral for Children Screening Positive for Mental Illness

MI
Start date: June 2004
Phase: Phase 0
Study type: Observational

The purpose of this study is to find out how prevalent unidentified Mental Health issues are in the pediatric population that visits the Emergency Department in an urban city.