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NCT01900964 · ClinicalTrials.gov registry record · NA
Ridge Preservation Comparing a PTFE Nonresorbable Membrane to a Collagen Membrane
A NA study, sponsored by University of Louisville.
- Completed
- Registry status
- NA
- Development phase
- 30
- Enrollment target
NCT01900964 is a NA study that has completed, run by University of Louisville. The registered enrollment target is 30 participants.
The verdict
NCT01900964, a NA study, has completed, sponsored by University of Louisville.
- COMPLETED
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
Study Summary
A non-resorbable PTFE (teflon) membrane will be compared to a resorbable collagen membrane when used for a post-extraction ridge preservation procedure to prevent the bone loss that typically occurs. The hypothesis is that there will be no difference in the clinical and histologic results between the two membranes.
Interventions
- PROCEDURE PTFE membrane
- PROCEDURE Collagen membrane
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2012-10 |
| Est. Completion | 2013-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01900964
The ClinicalTrials.gov registry entry for NCT01900964 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Louisville, which has 217 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which PTFE membrane is the first listed.
NCT01900964 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01900964 about?
NCT01900964 is a clinical study titled "Ridge Preservation Comparing a PTFE Nonresorbable Membrane to a Collagen Membrane". A non-resorbable PTFE (teflon) membrane will be compared to a resorbable collagen membrane when used for a post-extraction ridge preservation procedure to prevent the bone loss that typically occurs. The hypothesis is that there will be no difference in the clinical and histologic results between th...
What is the current status of trial NCT01900964?
This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2012-10. Estimated completion is 2013-11.
What interventions are being tested in trial NCT01900964?
The interventions under investigation include: PTFE membrane (PROCEDURE), Collagen membrane (PROCEDURE).
Who is sponsoring clinical trial NCT01900964?
This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.
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