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NCT00124501 · ClinicalTrials.gov registry record · NA
Effectiveness of Biofeedback-Assisted Relaxation Training in Children With Eosinophilic Duodenitis
A NA study of Abdominal Pain and Duodenitis, sponsored by Children's Mercy Hospital Kansas City.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT00124501 is a NA study of Abdominal Pain and Duodenitis that has completed, run by Children's Mercy Hospital Kansas City. The registered enrollment target is 20 participants, below the 149-participant average among 19 other Abdominal Pain trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00124501, a NA study of Abdominal Pain and Duodenitis, has completed, sponsored by Children's Mercy Hospital Kansas City.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine whether the addition of Biofeedback-Assisted Relaxation to standard medication treatment improves outcomes for children with a specific type of recurrent abdominal pain (i.e., eosinophilic gastroenteritis).
Conditions Studied
Interventions
- BEHAVIORAL Biofeedback-assisted relaxation training
Study Locations (1)
Missouri
- Children's Mercy Hospital - Kansas City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2004-10 |
| Est. Completion | 2006-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00124501
The ClinicalTrials.gov registry entry for NCT00124501 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 149-participant average among 19 other Abdominal Pain trials with a reported enrollment target (87% lower). The listed sponsor is Children's Mercy Hospital Kansas City, which has 184 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Abdominal Pain appearing as the primary indexed condition, and to 1 intervention - of which Biofeedback-assisted relaxation training is the first listed.
NCT00124501 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.
Frequently Asked Questions
What is clinical trial NCT00124501 about?
NCT00124501 is a clinical study titled "Effectiveness of Biofeedback-Assisted Relaxation Training in Children With Eosinophilic Duodenitis". The purpose of this study is to determine whether the addition of Biofeedback-Assisted Relaxation to standard medication treatment improves outcomes for children with a specific type of recurrent abdominal pain (i.e., eosinophilic gastroenteritis).
What is the current status of trial NCT00124501?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2004-10. Estimated completion is 2006-08.
What conditions does trial NCT00124501 study?
This clinical trial studies the following conditions: Abdominal Pain, Duodenitis.
What interventions are being tested in trial NCT00124501?
The interventions under investigation include: Biofeedback-assisted relaxation training (BEHAVIORAL).
Who is sponsoring clinical trial NCT00124501?
This trial is sponsored by Children's Mercy Hospital Kansas City, which has 184 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00124501 being conducted?
This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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