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Bone Graft
Bone Augmentation with Amnion Allograft and Allograft for Tooth Loss
N/A
Waitlist Available
Led By Maninder Kaur, BDS MPH
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 7 weeks, 12 months, 24 months,
Awards & highlights
Study Summary
This trial will compare the effects of two different materials used to regenerate bone in extraction sockets. One socket will be grafted with Bone Allograft and the other with Bone Allograft with Amnion. The investigators hypothesize that the Amnion graft will result in enhanced healing patterns and accelerated formation of regenerated bone.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 7 weeks, 12 months, 24 months,
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 7 weeks, 12 months, 24 months,
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Changes in Hard Tissue Composition
Secondary outcome measures
Changes in soft tissue healing
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Amnion AllograftExperimental Treatment1 Intervention
Atraumatic tooth extractions and amnion allograft procedures
Group II: AllograftActive Control1 Intervention
Atraumatic tooth extractions and allograft procedures
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Who is running the clinical trial?
University of Alabama at BirminghamLead Sponsor
1,584 Previous Clinical Trials
2,280,051 Total Patients Enrolled
BioDlogicsIndustry Sponsor
1 Previous Clinical Trials
2 Total Patients Enrolled
Maninder Kaur, BDS MPHPrincipal InvestigatorUniversity of Alabama at Birmingham
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are allergic to titanium.You are allergic to materials used for bone grafting.You are taking medications or have a medical condition that may harm the healing of your bones.You have one or more teeth in a visible area that need to be removed.You have had cancer in the past.
Research Study Groups:
This trial has the following groups:- Group 1: Amnion Allograft
- Group 2: Allograft
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any opportunities for participants to join this research endeavor?
"This study is no longer open for enrollment, as indicated by the clinicaltrials.gov listings which note that it was originally posted on 1/1/2013 and last updated 6/29/2022. Fortunately, 33 other trials are currently welcoming patients into their studies."
Answered by AI
Who else is applying?
What site did they apply to?
University of Alabama at Birmingham, School of Dentistry
What portion of applicants met pre-screening criteria?
Met criteria
How many prior treatments have patients received?
1
Why did patients apply to this trial?
I need top and bottom arches done.
PatientReceived 2+ prior treatments
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