Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 4 Interventional

STOP Trial - Sandostatin LAR Depot Trial for the Optimum Prevention of Chemotherapy Induced Diarrhea

ClinicalTrials.gov ID: NCT00050635

Public ClinicalTrials.gov record NCT00050635. 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 Oct 20, 2026, 7:38 AM EDT

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Currently there is an ongoing clinical trial for patients with chemotherapy induced diarrhea. This trial is being conducted to evaluate the efficacy of two dose levels (30 mg and 40 mg) of an investigational drug in reducing the occurrence of severe (Grade 3 or 4) diarrhea during chemotherapy. Eligible patients must either have experienced NCI Common Toxicity Grade 1 - 4 chemotherapy-induced diarrhea during previous chemotherapy treatment or be experiencing Grade 1-4 chemotherapy-induced diarrhea currently. In order to participate in this clinical trial, patients must be male or female 18 years of age or older. Inclusion into this investigational drug trial is based on the protocol entry criteria and a detailed evaluation from a participating trial investigator

Study identification

NCT ID
NCT00050635
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

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
Dec 2002 (Type not available)
Primary completion
Not listed
Completion
Jul 2003 (Type not available)
Last update posted
Nov 19, 2009

2002 – 2003

United States locations

U.S. sites
34
U.S. states
17
U.S. cities
34
Facility City State ZIP Site status
Kenmar Research Institute Burbank California 91505 —
Bay Area Cancer Research Group Concord California 94520 —
Compassionate Cancer Care medical Group, Inc. Fountain Valley California 92708 —
California Cancer Care, Inc. Greenbrae California 94904-2007 —
Pacific Shores Medical Center Long Beach California 90813 —
Kenmar Research Institute Los Angeles California 90057 —
Oncology Hematology Group of South Florida Miami Florida 33176 —
Pasco Hernando Oncology Associates New Port Richey Florida 34652 —
Mid-Florida Hematology & Oncology Centers, PA Orange City Florida 32763 —
Oncology & Hematology Associates of West Broward Tamarac Florida 33321 —
Creticos Cancer Center Chicago Illinois 60657 —
Decatur Memorial Hospital Decatur Illinois 62526 —
Cancer Care Center Bloomington Indiana 47403 —
Suniti Medical Corporation Merrillville Indiana 46410 —
Genesys Hurley Cancer Institute Flint Michigan 48503 —
Cancer & Hematology Centers of Western Michigan Grand Rapids Michigan 49546 —
Delta Oncology Greenwood Mississippi 38930 —
Missouri Cancer Associates Columbia Missouri 65201 —
Heartland Hematology Oncology Associates Kansas City Missouri 64118 —
Arch Medical Services/The Center for Cancer Care and Research St Louis Missouri 63141 —
New Mexico Cancer Care Associates Santa Fe New Mexico 87505 —
North Shore Hematology Oncology East Setauket New York 11733 —
Raleigh Hematology Oncology Associates, Wake Practice Raleigh North Carolina 27609 —
Dakota Clinic/Odyssey Research Services Fargo North Dakota 58103 —
Nashat Y. Gabrail, MD Canton Ohio 44718 —
North Coast Cancer Care, Inc. Sandusky Ohio 44870 —
Lawrence M. Stallings, MD Wooster Ohio 44691 —
Consultants in Medical Oncology-Hematology Drexel Hill Pennsylvania 19026 —
Regional Hematology Oncology Assoc Langhorne Pennsylvania 19047 —
Oncology Services of Aberdeen Borden South Dakota 57401 —
Jones Oncolgy/Hematology Clinic Germantown Tennessee 38138 —
McFaddin Ward Cancer - TOPA Beaumont Texas 77702 —
Scott & White Hospital/CCPC Waco Texas 76702 —
Oncology & Hematology Associates of SW VA Roanoke Virginia 24014 —

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 NCT00050635, 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 Nov 19, 2009 · Synced Oct 20, 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 public registry record, listed eligibility criteria, and available contact information for NCT00050635 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →