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Fever clinical trials

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NCT ID: NCT00598702 Completed - Pain Clinical Trials

Study of the Safety & Efficacy of Intravenous Acetaminophen in Pediatric Inpatients

Start date: January 2008
Phase: Phase 3
Study type: Interventional

Intravenous acetaminophen (IVAPAP) is safe in repeated dose, multi-day clinical use when administered at a daily dose of 40 to 75 mg/kg body weight

NCT ID: NCT00598559 Completed - Acute Pain Clinical Trials

Safety and Efficacy of Intravenous Acetaminophen (IV APAP) in Adult Inpatients

Start date: January 2008
Phase: Phase 3
Study type: Interventional

The study will be investigating safety and efficacy administration of repeated dose of IV Acetaminophen (IV APAP) over five days for the treatment of acute pain or fever in adult patients.

NCT ID: NCT00584454 Completed - Q Fever Clinical Trials

Safety Evaluation of a Q-fever Vaccine, NDBR 105

Start date: February 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety of Q Fever vaccine, NDBR 105, and collect data on incidence of occupational Q Fever infection in at risk personnel.

NCT ID: NCT00584194 Completed - Rift Valley Fever Clinical Trials

Safety and Immunogenicity Study of Rift Valley Fever Vaccine

RVF
Start date: June 2004
Phase: Phase 2
Study type: Interventional

This study is designed to determine the safety and immunogenicity of a Rift Valley Fever (RVF) Vaccine

NCT ID: NCT00582907 Completed - Clinical trials for Familial Mediterranean Fever

Rilonacept for Treatment of Familial Mediterranean Fever (FMF)

Start date: August 2008
Phase: Phase 2
Study type: Interventional

Familial Mediterranean fever (FMF) is a genetic disease resulting in recurrent attacks of fever, abdominal pain, chest pain, arthritis and rash. There are 5-15% of patients who continue to have FMF attacks despite treatment with colchicine or who cannot tolerate colchicine. Currently there are no alternatives to colchicine. Pyrin, the protein that has a defect in FMF has an important role in the regulation of a molecule called interleukin (IL)-1 beta production and activity. This molecule is very important in the process of inflammation in FMF. Therefore we propose to use IL-1 Trap (Rilonacept), a medication that binds and neutralizes IL-1. We will enroll in this study 17 subjects from the age of 4 years, including adults with active FMF despite colchicine therapy. Subjects will receive in random order two 3-month courses of Rilonacept at 2.2 mg/kg (maximum 160 mg) by weekly subcutaneous injection and two 3-month courses of placebo injection. If patients have at least two FMF attacks during a treatment course they will be able to get if they choose the other treatment until the end of that treatment course. Our hypothesis is that Rilonacept will decrease the number of acute FMF attacks and will be safe to use. This study may confirm the importance of IL-1 in the cause of FMF. Funding source - FDA Office of Orphan Products Development

NCT ID: NCT00568217 Completed - Clinical trials for Recurrence of Febrile Seizure

Antipyretics for Preventing Recurrences of Febrile Seizures

Start date: September 1997
Phase: Phase 4
Study type: Interventional

We wanted to find out if the early use of antipyretics is capable in preventing recurrences of febrile seizures. When a child has had his/her first febrile seizure, the parents were instructed to give him/her antipyretic medication every time when the child had a new episode of fever during two years.

NCT ID: NCT00565071 Recruiting - Malaria Clinical Trials

Parasite-based Diagnosis for Malaria in Uganda: Feasibility and Cost-Effectiveness

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

The purpose of this study is to compare the cost-effectiveness of treating malaria based on three methods of diagnosis (rapid test, microscopy and presumptive diagnosis) among patients attending level three government health centres located in areas of low and high transmission intensities in Uganda. The study hypotheses are: in both low and high transmission areas, cost-effectiveness of malaria treatment with Artemether-Lumefantrine will be improved by the adoption of rapid diagnostic tests when compared with presumptive diagnosis or microscopy; and the difference between the cost-effectiveness of Artemether-Lumefantrine treatment following rapid diagnostic test or microscopy versus presumptive diagnosis will be greatest in low transmission areas.

NCT ID: NCT00564629 Completed - Fever Clinical Trials

Study of the Efficacy and Safety of Intravenous vs Oral Acetaminophen for Treatment of Fever in Healthy Adult Males

Start date: August 2007
Phase: Phase 3
Study type: Interventional

To assess the rapidity of onset of antipyretic effect and the efficacy and safety of a single dose of IV acetaminophen (IV APAP) versus oral (PO) acetaminophen in the treatment of fever induced by a standard dose of endotoxin

NCT ID: NCT00536081 Completed - Breast Cancer Clinical Trials

Various G-CSF Regimens to Prevent Infection During Chemotherapy

Start date: January 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to prevent chemotherapy-related febrile neutropenia, prophylaxis with antibiotics and granulocyte colony-stimulating factor (G-CSF) have proven efficacious [1-3]. G-CSF has only few side effects, but is expensive. In 2006, updated G-CSF guidelines conclude that primary G-CSF prophylaxis has clinical benefits for and should be offered to patients at a more than 20% risk of febrile neutropenia. Based on many positive and few negative trials, one can consider the use of taxanes as standard of care in the adjuvant setting in node-positive breast cancer. Taxanes (with or without anthracyclines) have an increased risk for febrile neutropenia. The updated guidelines and changes in daily clinical practice will have a significant impact on the investigators health care resources. There is a higher risk of febrile neutropenia for the first chemotherapy cycle compared to subsequent cycles in small cell lung cancer patients. Also in advanced breast cancer the majority of first observed episodes of febrile neutropenia occur in the initial chemotherapy cycles Irrespective of tumour type or chemotherapy regimen, the risk of febrile neutropenia is highest during the first two cycles of chemotherapy. Thereafter, the risk rapidly declines, and the benefit of G-CSF largely seems to disappear. So, in order to improve the cost-effective administration of primary G-CSF prophylaxis, it is justified to assess whether G-CSF prophylaxis can be limited to the first two chemotherapy cycles as compared to the current practice of continuous G-CSF prophylaxis.

NCT ID: NCT00529282 Terminated - Fever Clinical Trials

A Study of Ceftobiprole in Patients With Fever and Neutropenia.

Start date: October 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of ceftobiprole versus a comparator in patients with fever and neutropenia