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Completed Phase 3 Interventional

Dronabinol Versus Standard Ondansetron Antiemetic Therapy in Preventing Delayed-Onset Chemotherapy-Induced Nausea and Vomiting

ClinicalTrials.gov ID: NCT00642512

Public ClinicalTrials.gov record NCT00642512. 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 27, 2026, 1:19 PM EDT

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

Official title

A Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Efficacy Study of Oral Dronabinol Alone and in Combination With Ondansetron Versus Ondansetron Alone in Subjects With Delayed Chemotherapy-Induced Nausea and Vomiting

Brief summary

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

The primary purpose of the study is to determine the efficacy of oral dronabinol versus standard ondansetron antiemetic therapy in preventing delayed-onset chemotherapy-induced nausea and vomiting (CINV) or retching by measuring the incidence of total response of nausea and vomiting and/or retching following administration of moderate-to-high emetogenic chemotherapeutic agents.

Study identification

NCT ID
NCT00642512
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
64 participants

Conditions and interventions

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
Jul 2003 (Type not available)
Primary completion
Jul 2004 (Actual)
Completion
Jul 2004 (Actual)
Last update posted
Apr 3, 2008

2003 – 2004

United States locations

U.S. sites
43
U.S. states
22
U.S. cities
40
Facility City State ZIP Site status
Site 970 Tucson Arizona — —
Site 950 Anaheim California — —
Site 925 Fountain Valley California — —
Site 913 Greenbrae California — —
Site 909 Los Angeles California — —
Site 908 Pomona California — —
Site 943 Rancho Mirage California — —
Site 932 Boynton Beach Florida — —
Site 924 Hollywood Florida — —
Site 940 Lakeland Florida — —
Site 921 New Port Richey Florida — —
Site 929 New Port Richey Florida — —
Site 933 Ormond Beach Florida — —
Site 922 Marietta Georgia — —
Site 928 Harvey Illinois — —
Site 914 Orland Park Illinois — —
Site 926 Skokie Illinois — —
Site 946 Springfield Illinois — —
Site 956 Terre Haute Indiana — —
Site 905 Southfield Michigan — —
Site 916 Fergus Falls Minnesota — —
Site 937 Greenwood Mississippi — —
Site 958 St Louis Missouri — —
Site 904 Missoula Montana — —
Site 919 Little Silver New Jersey — —
Site 920 Voorhees Township New Jersey — —
Site 948 Brooklyn New York — —
Site 953 Brooklyn New York — —
Site 910 The Bronx New York — —
Site 949 Valhalla New York — —
Site 947 Wilmington North Carolina — —
Site 902 Bismarck North Dakota — —
Site 942 Fargo North Dakota — —
Site 944 Columbus Ohio — —
Site 934 Oklahoma City Oklahoma — —
Site 931 Philadelphia Pennsylvania — —
Site 906 Pittsburgh Pennsylvania — —
Site 918 Charleston South Carolina — —
Site 923 North Charleston South Carolina — —
Site 917 Chattanooga Tennessee — —
Site 939 Chattanooga Tennessee — —
Site 915 Texarkana Texas — —
Site 951 Arlington Virginia — —

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 NCT00642512, 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 Apr 3, 2008 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00642512 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →