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NCT00881491 · ClinicalTrials.gov registry record · Early Phase 1
Treatment Outcome With a Revascularization Protocol Using the Triple Versus Double Antibiotic Paste
A Early Phase 1 study, sponsored by The University of Texas Health Science Center at San Antonio.
- Completed
- Registry status
- Early Phase 1
- Development phase
- 10
- Enrollment target
NCT00881491: Completed Early Phase 1 study, sponsored by The University of Texas Health Science Center at San Antonio.
NCT00881491 is a Early Phase 1 study that has completed, run by The University of Texas Health Science Center at San Antonio. The registered enrollment target is 10 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00881491, a Early Phase 1 study, has completed, sponsored by The University of Texas Health Science Center at San Antonio.
- COMPLETED
- Registry status
- Early Phase 1
- Development phase
- 10 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the treatment outcomes in permanent teeth with necrotic pulp and immature root development that undergo a regenerative procedure using a triple antibiotic paste (ciprofloxacin, metronidazole, minocycline) versus a double antibiotic paste (ciprofloxacin, metronidazole)compared to the commonly used mineral trioxide aggregate (MTA) apexification treatment.
Primary Outcome
1. st radiograph taken at 1 month post-procedure completion 2. nd radiograph taken at 3 month post-procedure completion 3. rd radiograph taken at 6 month post-procedure completion
Interventions
- DRUG Mineral Trioxide Aggregate
- DRUG Triple Antibiotic Paste
- DRUG Double Antibiotic Paste
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2009-04 |
| Est. Completion | 2015-01 |
| Phase | Early Phase 1 |
What the finished NCT00881491 record still lists
NCT00881491 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (81% lower).
The record links to 0 conditions, and to 3 interventions - of which Mineral Trioxide Aggregate is the first listed.
NCT00881491 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00881491 about?
NCT00881491 is a clinical study titled "Treatment Outcome With a Revascularization Protocol Using the Triple Versus Double Antibiotic Paste". The purpose of this study is to determine the treatment outcomes in permanent teeth with necrotic pulp and immature root development that undergo a regenerative procedure using a triple antibiotic paste (ciprofloxacin, metronidazole, minocycline) versus a double antibiotic paste (ciprofloxacin, metr...
What is the current status of trial NCT00881491?
This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 10 participants. The study started on 2009-04. Estimated completion is 2015-01.
What interventions are being tested in trial NCT00881491?
The interventions under investigation include: Mineral Trioxide Aggregate (DRUG), Triple Antibiotic Paste (DRUG), Double Antibiotic Paste (DRUG).
Who is sponsoring clinical trial NCT00881491?
This trial is sponsored by The University of Texas Health Science Center at San Antonio, which has 378 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00881491's enrollment target sits among peer trials
10 1629th of 2000 higher than 256 of 2,000 other Early Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Early Phase 1 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.
Source ClinicalTrials.gov registry export · 2026-08-08
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