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NCT01942304 · ClinicalTrials.gov registry record · NA

Prospective Evaluation of Anorganic Bovine Bone Mineral Versus Calcium Phosphosilicate Alloplastic Bone Putty in Direct Sinus Augmentation: a Spilt-mouth Study

A NA study, sponsored by University of Minnesota.

Completed
Registry status
NA
Development phase
12
Enrollment target

NCT01942304 is a NA study that has completed, run by University of Minnesota. The registered enrollment target is 12 participants.

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The verdict

NCT01942304, a NA study, has completed, sponsored by University of Minnesota.

COMPLETED
Registry status
NA
Development phase
12 participants
Enrollment target

Study Summary

The purpose of this split-mouth clinical study is to evaluate the clinical, radiographic and histological outcomes of lateral window sinus augmentation with a bovine xenograft or a CPS putty bone substitute in posterior maxillary sites and the survival of implants placed in these sites following healing.

Interventions

  • PROCEDURE Calcium phosphosilicate alloplastic bone putty in direct sinus augmentation
  • PROCEDURE Anorganic bovine bone mineral in direct sinus augmentation

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2013-10-01
Est. Completion 2019-05-31
Phase NA

Sponsor

University of Minnesota

966 total trials

What the Registry Record Tells You About NCT01942304

The ClinicalTrials.gov registry entry for NCT01942304 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Calcium phosphosilicate alloplastic bone putty in direct sinus augmentation is the first listed.

NCT01942304 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01942304 about?

NCT01942304 is a clinical study titled "Prospective Evaluation of Anorganic Bovine Bone Mineral Versus Calcium Phosphosilicate Alloplastic Bone Putty in Direct Sinus Augmentation: a Spilt-mouth Study". The purpose of this split-mouth clinical study is to evaluate the clinical, radiographic and histological outcomes of lateral window sinus augmentation with a bovine xenograft or a CPS putty bone substitute in posterior maxillary sites and the survival of implants placed in these sites following hea...

What is the current status of trial NCT01942304?

This trial is currently completed. It is a NA study. The enrollment target is 12 participants. The study started on 2013-10-01. Estimated completion is 2019-05-31.

What interventions are being tested in trial NCT01942304?

The interventions under investigation include: Calcium phosphosilicate alloplastic bone putty in direct sinus augmentation (PROCEDURE), Anorganic bovine bone mineral in direct sinus augmentation (PROCEDURE).

Who is sponsoring clinical trial NCT01942304?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.