Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00641316 · ClinicalTrials.gov registry record · NA

An Assessment of Bone Augmentation in Post-Extraction Sockets

A NA study, sponsored by University of Alabama at Birmingham.

Completed
Registry status
NA
Development phase
41
Enrollment target

NCT00641316: Completed NA study, sponsored by University of Alabama at Birmingham.

NCT00641316 is a NA study that has completed, run by University of Alabama at Birmingham. The registered enrollment target is 41 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00641316, a NA study, has completed, sponsored by University of Alabama at Birmingham.

COMPLETED
Registry status
NA
Development phase
41 participants
Enrollment target

Study Summary

When a tooth is extracted the ridge of bone that held the tooth in place begins to heal and over time new bone grows to fill the empty space left by the missing tooth. Sometimes this process works very well and new bone grows to completely fill the socket, at other times new bone fails to fill in the space completely and patients are left with uneven bone-fill. Grafted extraction sockets may fill with bone faster and more evenly than those without grafts, allowing the dentist to have greater control over the healing process and to repair the area with dental implants in a shorter period of time. This study will help determine if grafting an extraction socket, with or without enriching the graft material, is an added benefit when compared to allowing the socket to heal naturally. The study will also assess how well two different dental implant designs used to restore the area will function over time.

Primary Outcome

New bone formation in grafted extraction sockets to that of sites healed after 8 weeks of post-extraction.

Interventions

  • PROCEDURE AtraumaticTeeth Extraction
  • PROCEDURE Atraumatic Teeth Extraction/Grafted Extraction Sockets

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2008-04
Est. Completion 2012-11
Phase NA
University of Alabama at Birmingham

1,160 total trials

What the finished NCT00641316 record still lists

NCT00641316 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which AtraumaticTeeth Extraction is the first listed.

NCT00641316 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00641316 about?

NCT00641316 is a clinical study titled "An Assessment of Bone Augmentation in Post-Extraction Sockets". When a tooth is extracted the ridge of bone that held the tooth in place begins to heal and over time new bone grows to fill the empty space left by the missing tooth. Sometimes this process works very well and new bone grows to completely fill the socket, at other times new bone fails to fill in th...

What is the current status of trial NCT00641316?

This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2008-04. Estimated completion is 2012-11.

What interventions are being tested in trial NCT00641316?

The interventions under investigation include: AtraumaticTeeth Extraction (PROCEDURE), Atraumatic Teeth Extraction/Grafted Extraction Sockets (PROCEDURE).

Who is sponsoring clinical trial NCT00641316?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00641316's enrollment target sits among peer trials

41 1446th of 2000 higher than 554 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03449238 · 41 participants · Phase 1

    Pembrolizumab And Stereotactic Radiosurgery (Srs) Of Selected Brain Metastases In Breast Cancer Patients

  • NCT03900793 · 41 participants · Phase 1

    Losartan + Sunitinib in Treatment of Osteosarcoma

  • NCT04082520 · 41 participants · Phase 2

    Lutathera for the Treatment of Inoperable, Progressive Meningioma After External Beam Radiation Therapy

  • NCT04220190 · 41 participants · Phase 2

    RAPA-501 Therapy for ALS

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00641316, the US trial registry maintained by the National Library of Medicine. NCT00641316 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.