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A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients Clinical Trials Facts presented on Clinical Trials Search is not designed to be a substitute for certified medical advice, travels to or treatment with a real dr.. We aren't doctors. Always consult your mD on A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients conditions. Clinical Trials Search.org is a website dedicated to listing clinical research studies in human subjects. A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients Clinical research trials and A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients medical trials occur in many of places across the U.S.A.. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials generally assess the effectiveness of new does drugs. The role of the studies / undertakings is to figure out certain human healthcare questions. Clinical trials are a popular means for doctors, government agencies, and private sector corporations to locate treatments for all forms of circumstances, including A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients. A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients Clinical Trials and other clinical trials permit volunteers to get medical treatment options before they are available to the masses. Most times the human subjects acquire treatment for free of charge, and sometimes they are paid for their time. Occasionally there is a cost for a A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients clinical trial. Participants oftentimes recieve the finest healthcare available for their A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients condition. Dangers are a reality, nonetheless, and might include extra or frequent physician calls, health hazards (potentially life-endangering), and/or the treatment being ineffectual. Trials are federally regulated with strict guidelines to protect clinical trials subjects.

Home > "A" Clinical Trials Conditions > A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients

A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients



A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients

For Condition: Pneumonia, Pneumocystis carinii,HIV Infections
Status: No longer recruiting
Sponsor(s): National Institute of Allergy and Infectious Diseases (NIAID) , Glaxo Wellcome
Synopsis: To compare the safety and efficacy of two dosage regimens (daily and thrice-weekly) of sulfamethoxazole/trimethoprim (SMX/TMP; TMS) in the prevention of Pneumocystis carinii pneumonia (PCP) in high-risk HIV-infected patients. Previous tests have shown that SMX/TMP given daily is effective in preventing recurrence of PCP and may be effective in preventing PCP in patients who have never developed it. Because SMX/TMP can cause side effects, this study will attempt to determine the safest and most effective dose of this combination.
Details: Previous tests have shown that SMX/TMP given daily is effective in preventing recurrence of PCP and may be effective in preventing PCP in patients who have never developed it. Because SMX/TMP can cause side effects, this study will attempt to determine the safest and most effective dose of this combination. Patients receive SMX/TMP orally on a daily or thrice-weekly basis. Patients are clinically evaluated every 4 months. Patients on daily SMX/TMP who develop a drug-related toxicity may be switched to thrice-weekly SMX/TMP. Duration of follow-up is 12 months.
Eligibility:
Study Type:
  Interventional, Treatment, Parallel Assignment, Safety Study
Minimum Age/Maximum Age: 13 Years/
Genders: Both
Protocol Entry Criteria: Inclusion Criteria Patients must have: - HIV infection. - CD4 count <= 200 cells/mm3 OR a history of prior PCP. - No active pneumocystosis. Patients or their guardians must sign informed consent. Pregnant patients are eligible at the clinician's discretion. Patients who do not meet required laboratory values may be eligible at the discretion of the clinician. Exclusion Criteria Co-existing Condition: Patients with the following symptoms and conditions are excluded: - Known treatment-limiting reaction to sulfonamides or trimethoprim. Concurrent Medication: Excluded: - Other PCP prophylaxis or medication with anti-PCP activity.
Total Enrollment: 2500

Location and Contact Information:

Overall Study Official:
WEl-Sadr,  Study Chair, 

Wilmington Hosp / Med Ctr of Delaware
Wilmington,  Delaware,  19899
United States
 

Comprehensive AIDS Alliance of Detroit
Detroit,  Michigan,  48201
United States
 

Richmond AIDS Consortium
Richmond,  Virginia,  23298
United States
 

Stanford Univ School of Medicine
Stanford,  California,  943055107
United States
 

Harlem AIDS Treatment Group / Harlem Hosp Ctr
New York City,  New York,  10037
United States
 

Clinical Directors Network of Region II
New York City,  New York,  10011
United States
 

Community Consortium of San Francisco
San Francisco,  California,  94110
United States
 

North Jersey Community Research Initiative
Newark,  New Jersey,  071032842
United States
 

Philadelphia FIGHT
Philadelphia,  Pennsylvania,  19107
United States
 

Baltimore Trials
Baltimore,  Maryland,  21201
United States
 

Partners Research
Albuquerque,  New Mexico,  871315271
United States
 

Univ of Washington / Pacific Med Ctr
Seattle,  Washington,  98144
United States
 

AIDS Research Consortium of Atlanta
Atlanta,  Georgia,  30308
United States
 

Portland Veterans Adm Med Ctr / Rsch & Education Grp
Portland,  Oregon,  972109951
United States
 

Southern New Jersey AIDS Cln Trials / Dept of Med
Camden,  New Jersey,  08103
United States
 

Univ of Maryland at Baltimore
Baltimore,  Maryland,  21201
United States
 

AIDS Research Alliance - Chicago
Chicago,  Illinois,  60657
United States
 

Veterans Administration Med Ctr / Regional AIDS Program
Washington D.C.,  District of Columbia,  20422
United States
 

Henry Ford Hosp
Detroit,  Michigan,  48202
United States
 

Addiction Research and Treatment Corp
Brooklyn,  New York,  11201
United States
 

Univ Hosp / HIV - ID Clinic
Albuquerque,  New Mexico,  87131
United States
 

Denver CPCRA / Denver Public Hlth
Denver,  Colorado,  802044507
United States
 

Bronx Lebanon Hosp Ctr
Bronx,  New York,  10456
United States
 

Louisiana Comm AIDS Rsch Prog / Tulane Univ Med
New Orleans,  Louisiana,  70112
United States
 


Additional Information:
Study ID Numbers:
  CPCRA 006; 
Study Start Date: 
Record last reviewed: January 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000748

Other Pneumonia, Pneumocystis Carinii Studies:
1. A Double-Blind, Randomized, Placebo-Controlled, Multicenter Study to Assess the Efficacy and Safety of Orally Administered SP-303 for the Treatment of Diarrhea in Acquired Immunodeficiency Syndrome (AIDS) Patients

2. The Effectiveness of Nelfinavir and Efavirenz, Used Alone or Together, Combined with Other Anti-HIV Drugs in Patients Who Have Taken Anti-HIV Drugs

3. A Controlled Comparative Trial of Sulfamethoxazole-Trimethoprim Versus Aerosolized Pentamidine for Secondary Prophylaxis of Pneumocystis carinii Pneumonia in AIDS Patients Receiving Azidothymidine (AZT)

4. A Phase II Trial of rsCD4 and AZT in Patients With AIDS or Advanced AIDS Related Complex (ARC)

5. Evaluation and Natural History of Children with Cancer and AIDS

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A Randomized, Comparative, Prospective Study of Daily Trimethoprim / Sulfamethoxazole (TMS) and Thrice-Weekly TMS for Prophylaxis Against PCP in HIV-Infected Patients

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