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NCT00046865 · ClinicalTrials.gov registry record · Phase 3
Acupressure in Treating Nausea in Women Receiving Combination Chemotherapy for Breast Cancer
A Phase 3 study of Breast Cancer and Drug-induced Nausea and Vomiting, sponsored by M.D. Anderson Cancer Center.
- Completed
- Registry status
- Phase 3
- Development phase
- 57
- Enrollment target
- 2
- Study locations
NCT00046865 is a Phase 3 study of Breast Cancer and Drug-induced Nausea and Vomiting that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 57 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT00046865, a Phase 3 study of Breast Cancer and Drug-induced Nausea and Vomiting, has completed, sponsored by M.D. Anderson Cancer Center.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 57 participants
- Enrollment target
- 2
- Study locations
Study Summary
RATIONALE: Acupressure may help to reduce or prevent nausea in patients who are undergoing chemotherapy. It is not yet known whether acupressure plus standard care for nausea is more effective than standard care alone for nausea in women who are receiving chemotherapy for breast cancer. PURPOSE: Randomized phase III trial to determine the effectiveness of acupressure in treating nausea in women who are receiving combination chemotherapy for breast cancer.
Conditions Studied
Interventions
- PROCEDURE management of therapy complications
- PROCEDURE acupressure therapy
- PROCEDURE nausea and vomiting therapy
Study Locations (2)
Florida
- H. Lee Moffitt Cancer Center CCOP Research Base - Tampa
Texas
- University of Texas M.D. Anderson CCOP Research Base - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 57 participants |
| Start Date | 2002-07-01 |
| Est. Completion | 2006-03-23 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00046865
The ClinicalTrials.gov registry entry for NCT00046865 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 57 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Breast Cancer appearing as the primary indexed condition, and to 3 interventions - of which management of therapy complications is the first listed.
NCT00046865 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Florida, Texas.
Frequently Asked Questions
What is clinical trial NCT00046865 about?
NCT00046865 is a clinical study titled "Acupressure in Treating Nausea in Women Receiving Combination Chemotherapy for Breast Cancer". RATIONALE: Acupressure may help to reduce or prevent nausea in patients who are undergoing chemotherapy. It is not yet known whether acupressure plus standard care for nausea is more effective than standard care alone for nausea in women who are receiving chemotherapy for breast cancer. PURPOSE: Ra...
What is the current status of trial NCT00046865?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 57 participants. The study started on 2002-07-01. Estimated completion is 2006-03-23.
What conditions does trial NCT00046865 study?
This clinical trial studies the following conditions: Breast Cancer, Drug-induced Nausea and Vomiting.
What interventions are being tested in trial NCT00046865?
The interventions under investigation include: management of therapy complications (PROCEDURE), acupressure therapy (PROCEDURE), nausea and vomiting therapy (PROCEDURE).
Who is sponsoring clinical trial NCT00046865?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00046865 being conducted?
This trial has 2 study locations across Florida, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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