New study tests better way to rebuild jawbone for dental implants
NCT ID NCT07613047
First seen Jun 06, 2026
Summary
This study compares two barrier materials used in guided bone regeneration to rebuild the jawbone in areas where teeth are missing. Seventy adults needing horizontal ridge augmentation will be randomly assigned to receive either acellular dermal matrix or a resorbable collagen membrane. The goal is to see which material better restores bone width and improves soft tissue outcomes for future dental implants.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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University of Alabama at Birmingham
Birmingham, Alabama, 35294, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
acellular dermal matrix (AlloDerm) and resorbable cross-linked collagen membrane
What this could lead to
If successful, this could show that acellular dermal matrix is a better option for rebuilding jawbone width, potentially improving dental implant success.
What could go wrong
This is an early-stage study with only 70 participants, so results may not apply to everyone. The procedure involves surgery with risks like pain, swelling, or infection.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.