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ClinicalTrials.gov record
Completed Not applicable Interventional

A Multicenter Placebo-Controlled Double Blind Study to Evaluate the Efficacy and Safety of Sandostatin ( SMS 201-995 ) in Patients With Acquired Immunodeficiency Related Diarrhea Who Were Either "Responders" or "Non-Responders" in a Prior Placebo-Controlled Double-Blind Sandostatin Study.

ClinicalTrials.gov ID: NCT00002253

Public ClinicalTrials.gov record NCT00002253. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 6:04 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT00002253
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Sandoz
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • Octreotide Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 23, 2005

United States locations

U.S. sites
22
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
USC School of Medicine Los Angeles California 90033
UCSD Med Ctr San Diego California 92103
UCSF - San Francisco Gen Hosp San Francisco California 94110
Kaiser Permanente Med Ctr San Francisco California 94115
San Mateo County Gen Hosp San Mateo California 94403
Med Service Miami Florida 33125
Emory Univ School of Medicine Atlanta Georgia 30303
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612
Maine Med Ctr Med Clinics Portland Maine 04102
Douglas Plesko Boston Massachusetts 02115
Boston City Hosp Boston Massachusetts 02118
Henry Ford Hosp Detroit Michigan 48202
Univ of Missouri at Kansas City School of Medicine Kansas City Missouri 64108
Mount Sinai Med Ctr New York New York 10029
SUNY Stony Brook / Health Sciences Ctr Stony Brook New York 117948121
Portland Veterans Adm Med Ctr / Rsch & Education Grp Portland Oregon 97210
Buckley Braffman Stern Med Associates Philadelphia Pennsylvania 19107
Miriam Hosp / Family Healthcare Ctr at SSTAR Providence Rhode Island 02906
Univ TX Galveston Med Branch Galveston Texas 77550
Baylor College of Medicine Houston Texas 77030
Infectious Disease Physicians Inc Annandale Virginia 22203
Univ of Wisconsin School of Medicine Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00002253, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 23, 2005 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00002253 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →