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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 Clinical Trials References presented on Clinical Trials Search isn't meant to be a substitute for proven healthcare advice, trips or professional assistance using a genuine physician. We are not docs. Always confer with your physician about 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 conditions. Clinical Trials Search.org is a site devoted to listing clinical research studies in human subjects. 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 Clinical research trials and 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 healthcare trials happen in hundreds of localities throughout the United States of America. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials usually evaluate the potency of new drugs. The propose of the studies / projects is to answer particular human health questions. Clinical trials are a popular way for mDs, government agencies, and private sector companies to detect cures for all sorts of conditions, such as 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. 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 Clinical Trials and other clinical trials allow volunteers to acquire healthcare treatment choices before they are available to the general public. Some times the subjects recieve professional assistance for free, and every now and again they are compensated for their time. Sometimes there is a cost for a 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 clinical trial. Subjects frequently obtain the most expert healthcare possible for their 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 condition. Risks are a reality, nevertheless, and can include more or frequent doctor trips, medical risks (possibly life-threatening), and/or the treatment being uneffective. Trials are federally governed with stern guidelines to protect clinical trials patients.

Home > "A" Clinical Trials Conditions > 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

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



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

For Condition: Diarrhea,HIV Infections
Status: Completed
Sponsor(s): Shaman Pharmaceuticals ,
Synopsis: To evaluate the efficacy, safety, and durability of response of SP-303 in decreasing stool weight in AIDS patients with diarrhea over 6 days of treatment.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Double-Blind, Safety Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: Inclusion Criteria Patients must have: - HIV infection meeting CDC criteria for AIDS. - History of diarrhea for greater than or equal to 14 days prior to screening period (Day 1). Required: On stable medical regimen.
Total Enrollment: 300

Location and Contact Information:

Oak Park Hosp
Oak Park,  Illinois,  60304
United States
 

GCRC
Washington D.C.,  District of Columbia,  20060
United States
 

Ctr for Quality Care
Tampa,  Florida,  33609
United States
 

San Francisco Gen Hosp
San Francisco,  California,  94110
United States
 

Washington Univ School of Medicine
St. Louis,  Missouri,  63110
United States
 

UCLA Care Ctr
Los Angeles,  California,  90095
United States
 

Phoenix Living Ctr
Scottsdale,  Arizona,  85251
United States
 

South Texas Veterans Health Care System
San Antonio,  Texas,  78284
United States
 

Wayne State Univ
Detroit,  Michigan,  48201
United States
 

New Orleans Pharmaceutical Research
Kenner,  Louisiana,  70062
United States
 

Johns Hopkins Hosp
Baltimore,  Maryland,  212875554
United States
 

Deering Hosp
Miami,  Florida,  33157
United States
 

Central Florida Research Initiative
Maitland,  Florida,  32751
United States
 

New England Med Ctr
Boston,  Massachusetts,  02111
United States
 

Howard Univ
Washington D.C.,  District of Columbia,  20059
United States
 

Rosemont Health Care Ctr
Orlando,  Florida,  32808
United States
 

Brookdale Univ Hosp and Med Ctr
Brooklyn,  New York,  112123198
United States
 

Clinical Research Puerto Rico Inc
San Juan,  ,  00909
Puerto Rico
 

Joseph Gathe
Houston,  Texas,  77004
United States
 

Wake Med CRI
Raleigh,  North Carolina,  27610
United States
 

GCRC - VA Hosp
San Antonio,  Texas,  78284
United States
 

Indiana Univ Med Ctr
Indianapolis,  Indiana,  462025250
United States
 

Lynn House Hospice
West Hollywood,  California,  90046
United States
 

Community CRI of South Florida
Coral Gables,  Florida,  33146
United States
 

Hill Top Research Ltd
Scottsdale,  Arizona,  85251
United States
 

Bailey Boushay House
Seattle,  Washington,  98112
United States
 

AIDS Research Alliance
West Hollywood,  California,  90069
United States
 

Regions Hosp
St. Paul,  Minnesota,  55101
United States
 

Saint Vincents Hosp
New York City,  New York,  10011
United States
 

Insite Clinical Trials
Decatur,  Georgia,  30033
United States
 

Phillip Branchman
Atlanta,  Georgia,  30327
United States
 

Rosehedge House
Seattle,  Washington,  98125
United States
 

Mem Hosp of Tampa
Tampa,  Florida,  33609
United States
 

AIDS Research Ctr / Dept of Veterans Affairs
Palo Alto,  California,  94304
United States
 

Hennepin County Med Ctr
Minneapolis,  Minnesota,  55415
United States
 

Hosp Regional de Ponce
Ponce,  ,  00731
Puerto Rico
 


Additional Information:
Study ID Numbers:
  293A;  37,554-210
Study Start Date: 
Record last reviewed: April 1999
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00002408

Other Hiv Infections Studies:
1. A Multicenter Placebo-Controlled Dose Titration Study to Evaluate the Efficacy and Safety of Sandostatin (SMS 201-995) in the Treatment of Patients With Acquired Immunodeficiency Related Diarrhea

2. Pentosan Polysulfate in Treating Patients With Gastrointestinal Disturbance Caused by Radiation Therapy

3. Octreotide in Preventing Diarrhea in Patients Receiving Chemotherapy for Colorectal Cancer

4. A Randomized Trial of Tap Water Treatment in the Elderly

5. Genetic Trial to Study Diarrhea in Patients With Stage III Colon Cancer Who Are Receiving Chemotherapy

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