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NCT01346267 · ClinicalTrials.gov registry record · NA
Acupressure in Controlling Nausea in Young Patients Receiving Highly Emetogenic Chemotherapy
A NA study of Unspecified Childhood Solid Tumor, Protocol Specific and Chemotherapy-induced Nausea and Vomiting, sponsored by University of South Florida.
- Completed
- Registry status
- NA
- Development phase
- 187
- Enrollment target
- 20
- Study locations
NCT01346267: Completed NA study of Unspecified Childhood Solid Tumor, Protocol Specific and Chemotherapy-induced Nausea and Vomiting, sponsored by University of South Florida.
NCT01346267 is a NA study of Unspecified Childhood Solid Tumor, Protocol Specific and Chemotherapy-induced Nausea and Vomiting that has completed, run by University of South Florida. The registered enrollment target is 187 participants, below the 1,623-participant average among 13 other Unspecified Childhood Solid Tumor, Protocol Specific trials with a reported enrollment target (88% lower). The trial reports 20 study locations across 13 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01346267, a NA study of Unspecified Childhood Solid Tumor, Protocol Specific and Chemotherapy-induced Nausea and Vomiting, has completed, sponsored by University of South Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 187 participants
- Enrollment target
- 20
- Study locations
Study Summary
RATIONALE: Acupressure wristbands may prevent or reduce nausea and caused by chemotherapy. It is not yet known whether standard care is more effective with or without acupressure wristbands in controlling acute and delayed nausea. PURPOSE: This randomized phase III trial is studying how well acupressure wristbands work with or without standard care in controlling nausea in young patients receiving highly emetogenic chemotherapy.
Primary Outcome
CIN = Chemotherapy-Induced Nausea. The acute phase began with administration of the first chemotherapy dose of a chemotherapy block and continued until 24 hours after administration of the last chemotherapy dose of the block. Acute Phase - bands will be worn on each day of the chemotherapy course and for 24 hours after the last chemotherapy dose. Nausea severity during the acute phase of chemotherapy is defined as the maximum PeNAT (Pediatric Nausea Assessment Tool) score observed during each 24
Conditions Studied
Interventions
- PROCEDURE Real Acupressure Band
- PROCEDURE Placebo Acupressure Band
Study Locations (20)
Florida
- Children's Hospital of Southwest Florida at Lee Memorial - Fort Myers
- Nemours Children's Clinic - Jacksonville
- Palms West Hospital - Loxahatchee Groves
- Nemours Children's Clinic - Orlando - Orlando
- Nemours Children's Clinic - Pensacola - Pensacola
- All Children's Hospital - St. Petersburg
- Tampa General Hospital - Tampa
California
- Miller Children's Hospital - Long Beach
- Childrens Hospital Los Angeles - Los Angeles
Connecticut
- Connecticut Children's Medical Center - Hartford
Delaware
- A I duPont Hospital for Children - Wilmington
District of Columbia
- Childrens National Medical Center - Washington D.C.
Hawaii
- Kapiolani Medical for Women and Children - Honolulu
Louisiana
- Ochsner Clinic Foundation New Orleans - New Orleans
Massachusetts
- Dana Farber Cancer Institute at Boston Children's Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 187 participants |
| Start Date | 2011-05 |
| Est. Completion | 2016-05 |
| Phase | NA |
What the finished NCT01346267 record still lists
NCT01346267 is an interventional study that assigns participants to a tested intervention. The registered 187 participants enrollment target is mid-sized for trials with a published cap, below the 1,623-participant average among 13 other Unspecified Childhood Solid Tumor, Protocol Specific trials with a reported enrollment target (88% lower).
The record links to 3 conditions, with Unspecified Childhood Solid Tumor, Protocol Specific appearing as the primary indexed condition, and to 2 interventions - of which Real Acupressure Band is the first listed.
NCT01346267 names 20 study sites across 13 states, led by Florida, California, Connecticut.
Frequently Asked Questions
What is clinical trial NCT01346267 about?
NCT01346267 is a clinical study titled "Acupressure in Controlling Nausea in Young Patients Receiving Highly Emetogenic Chemotherapy". RATIONALE: Acupressure wristbands may prevent or reduce nausea and caused by chemotherapy. It is not yet known whether standard care is more effective with or without acupressure wristbands in controlling acute and delayed nausea. PURPOSE: This randomized phase III trial is studying how well acupre...
What is the current status of trial NCT01346267?
This trial is currently completed. It is a NA study. The enrollment target is 187 participants. The study started on 2011-05. Estimated completion is 2016-05.
What conditions does trial NCT01346267 study?
This clinical trial studies the following conditions: Unspecified Childhood Solid Tumor, Protocol Specific, Chemotherapy-induced Nausea and Vomiting, Central Nervous System Tumor, Pediatric.
What interventions are being tested in trial NCT01346267?
The interventions under investigation include: Real Acupressure Band (PROCEDURE), Placebo Acupressure Band (PROCEDURE).
Who is sponsoring clinical trial NCT01346267?
This trial is sponsored by University of South Florida, which has 252 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01346267 being conducted?
This trial has 20 study locations across California, Connecticut, Delaware, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Unspecified Childhood Solid Tumor, Protocol Specific
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01346267's enrollment target sits among peer trials
187 4th of 13 higher than 10 of 13 other Unspecified Childhood Solid Tumor, Protocol Specific trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Unspecified Childhood Solid Tumor, Protocol Specific trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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