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NCT ID: NCT00216385 Recruiting - Tuberculosis Clinical Trials

A Controlled Trial of a 4-Month Quinolone-Containing Regimen for the Treatment of Pulmonary Tuberculosis

Start date: January 2005
Phase: Phase 3
Study type: Interventional

Tuberculosis is currently treated with a 6-month course regimen. During this time many patients might fail to adhere to treatment and default, increasing the risk of recurrent disease which might be multidrug resistant. A shorter duration of treatment is expected to provide improved patient compliance and at least equal or better clinical outcome. The aim of the trial is to evaluate the efficacy and safety of a gatifloxacin-containing regimen of four months duration for the treatment of pulmonary tuberculosis,

NCT ID: NCT00203762 Recruiting - Tuberculosis Clinical Trials

Effect of Public Sector Antiretroviral Treatment Programme on Tuberculosis and Immunization Care

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

A scale-up of public sector antiretroviral treatment (ART) programmes may divert scarce resources from other priority primary care programmes like tuberculosis and childhood immunization. The purpose of this study is to compare the performance of tuberculosis (TB) and childhood immunization programmes in primary care facilities participating in the South African national antiretroviral treatment programme with those which have yet to be included in the ART programme.

NCT ID: NCT00136370 Recruiting - Sepsis Clinical Trials

Prevention of Perinatal Sepsis (PoPS): Evaluation of Chlorhexidine Wipes of Birth Canal and Newborn

Start date: April 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate whether use of the disinfectant chlorhexidine administered to the birth canal during labour and newborn at delivery can protect a woman and her baby from bacterial infections after birth. If effective, this could be used as an inexpensive alternative to antibiotics to prevent newborn infections in resource-poor countries.

NCT ID: NCT00122746 Recruiting - Clinical trials for Cancer of the Cervix

Clinical and Experimental Studies to Improve Radiotherapy Outcome in AIDS Cancer Patients

Start date: December 2004
Phase: Phase 3
Study type: Interventional

The researchers plan: - To undertake clinical studies of radiotherapy with or without the administration of the chemotherapeutic agent cisplatin, known to be a radiosensitizer; - To perform pre-clinical studies of the radiosensitivity of human fibroblasts and cervical cancer cell lines in culture, with or without the addition of various HIV proteins or protease inhibitors, in order to determine the extent of any cellular radiosensitizing properties of these molecules; - To develop strategies for sensitizing tumour cells to radiation, specifically by down-regulating specific viral proteins that are known to be factors associated with resistance to radiotherapy.

NCT ID: NCT00117728 Recruiting - HIV Infections Clinical Trials

Pediatric Nevirapine Resistance Study

Start date: April 2005
Phase: Phase 3
Study type: Interventional

This study is designed to test if a sequential protease-inhibitor (PI) - / nevirapine (NVP) -based regimen is effective for the treatment of HIV-infected children when previous NVP exposure has occurred as part of programs to prevent mother-to-child transmission (pMTCT).

NCT ID: NCT00017992 Recruiting - HIV Infections Clinical Trials

Emtricitabine Given Once A Day With Other Anti-HIV Drugs in Children With HIV

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see if emtricitabine is safe in children infected with HIV and to determine the best dose.