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NCT00257946 · ClinicalTrials.gov registry record · Phase 3
Type of Material in Repair of Congenital Diaphragmatic Hernia
A Phase 3 study, sponsored by Children's Mercy Hospital Kansas City.
- Terminated
- Registry status
- Phase 3
- Development phase
- 50
- Enrollment target
NCT00257946 is a Phase 3 study that was terminated before completion, run by Children's Mercy Hospital Kansas City. The registered enrollment target is 50 participants.
The verdict
NCT00257946, a Phase 3 study, was terminated before completion, sponsored by Children's Mercy Hospital Kansas City.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 50 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the use of 2 different types of biosynthetic material for the repair of congenital diaphragmatic hernia. The research question is: what is the best material for repairing large congenital diaphragmatic hernias? The primary outcome variable is recurrence.
Interventions
- PROCEDURE Repair of CDH w/SIS Gold
- PROCEDURE Repair of CDH w/Alloderm
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2005-12 |
| Est. Completion | 2007-08 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00257946
The ClinicalTrials.gov registry entry for NCT00257946 describes a study currently listed as terminated, categorized as Phase 3. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Mercy Hospital Kansas City, which has 184 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Repair of CDH w/SIS Gold is the first listed.
NCT00257946 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00257946 about?
NCT00257946 is a clinical study titled "Type of Material in Repair of Congenital Diaphragmatic Hernia". The objective of this study is to evaluate the use of 2 different types of biosynthetic material for the repair of congenital diaphragmatic hernia. The research question is: what is the best material for repairing large congenital diaphragmatic hernias? The primary outcome variable is recurrence.
What is the current status of trial NCT00257946?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 50 participants. The study started on 2005-12. Estimated completion is 2007-08.
What interventions are being tested in trial NCT00257946?
The interventions under investigation include: Repair of CDH w/SIS Gold (PROCEDURE), Repair of CDH w/Alloderm (PROCEDURE).
Who is sponsoring clinical trial NCT00257946?
This trial is sponsored by Children's Mercy Hospital Kansas City, which has 184 total clinical trials registered on ClinicalTrials.gov.
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