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NCT02174198 · ClinicalTrials.gov registry record · NA

Bone Remodeling After Immediate Implant Placement With and Without Bone Grafting

A NA study, sponsored by Columbia University.

Completed
Registry status
NA
Development phase
32
Enrollment target

NCT02174198: Completed NA study, sponsored by Columbia University.

NCT02174198 is a NA study that has completed, run by Columbia University. The registered enrollment target is 32 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02174198, a NA study, has completed, sponsored by Columbia University.

COMPLETED
Registry status
NA
Development phase
32 participants
Enrollment target

Study Summary

This study compares two ways of placing a dental implant on the day of tooth extraction. One method will place a additional bone graft (derived from bovine bone) and the other group will not have the graft placed. Both groups will be restored at the same time with an immediate crown. The investigators will be researching and comparing the changes in gum level that occur after each surgical method, as well as changes in jaw width where the implant is placed. The investigators will enroll 16 patients per group. The patients will be followed for 3, 6, and 12 months post-immediate implant placement to observe healing.

Primary Outcome

The horizontal dimensional change from a digital superimposition at 3mm apical to the baseline free gingival margin position was measured.

Interventions

  • DEVICE BioOss Collagen at the time of implant placement

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2014-01
Est. Completion 2018-08
Phase NA
Columbia University

958 total trials

What the finished NCT02174198 record still lists

NCT02174198 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which BioOss Collagen at the time of implant placement is the first listed.

NCT02174198 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02174198 about?

NCT02174198 is a clinical study titled "Bone Remodeling After Immediate Implant Placement With and Without Bone Grafting". This study compares two ways of placing a dental implant on the day of tooth extraction. One method will place a additional bone graft (derived from bovine bone) and the other group will not have the graft placed. Both groups will be restored at the same time with an immediate crown. The investigat...

What is the current status of trial NCT02174198?

This trial is currently completed. It is a NA study. The enrollment target is 32 participants. The study started on 2014-01. Estimated completion is 2018-08.

What interventions are being tested in trial NCT02174198?

The interventions under investigation include: BioOss Collagen at the time of implant placement (DEVICE).

Who is sponsoring clinical trial NCT02174198?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02174198's enrollment target sits among peer trials

32 1578th of 2000 higher than 409 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

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Source: ClinicalTrials.gov NCT02174198, the US trial registry maintained by the National Library of Medicine. NCT02174198 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.