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Bioactive Glass (Sol-gel) for Alveolar Bone Regeneration After Surgical Extraction

NCT01878084 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2020-02-18

Study results available
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Summary

The purpose of the present research is to evaluate the effect of bioactive glass in bone regeneration immediately following extraction of mandibular and maxillary premolars.The hypothesis of the study assumes that this treatment would promote the healing of the extraction socket while preserving both the height and width of the bone. Furthermore, it would allow more effective tooth movement during orthodontic treatment.

Conditions

  • Bone Loss
  • Vertical Alveolar Bone Loss
  • Horizontal Alveolar Bone Loss

Interventions

OTHER

bioactive glass (sol-gel)

Extraction sockets will be augmented using bioactive glass (sol-gel)

OTHER

empty extraction socket

Extraction socket will be left empty

Sponsors & Collaborators

  • Lehigh University

    collaborator OTHER

  • Alexandria University

    lead OTHER

Principal Investigators

  • Mona Marei, prof · Alexandria University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
9 Years
Max Age
16 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2016-12-31
Completion
2018-01-31

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01878084 on ClinicalTrials.gov