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Clinical Trials/CTRI/2020/06/025567
CTRI/2020/06/025567
Recruiting
Phase 1

Evaluating The Efficacy of Sticky Bone In Horizontal Ridge Augmentation with and without membrane: A Randomized Parallel arm Clinical Trial

Jane BelindaT0 sites0 target enrollmentTBD
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Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Jane BelindaT
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Jane BelindaT

Eligibility Criteria

Inclusion Criteria

  • •1\.Patients who are between 18\-60 years of age.
  • •2\.All sites had to be healed sites, that is at least 6 months of post extraction healing was required.
  • •3\.Each site bordered by at least one tooth.
  • •4\.Single edentulous sites were the treatment planned to receive a dental implant that was evaluated to have inadequate horizontal dimensions for implant placement and classified as either Seibert Class I or III.

Exclusion Criteria

  • •1\.Debilitating systemic diseases or diseases that have a clinically significant effect on wound healing.
  • •2\.History of intravenous bisphosphonate use or oral bisphosphonate use for \>3 years
  • •3\.Smokers.
  • •4\.Pregnancy or lactation
  • •5\.Known allergy to any material or medication used in the study.
  • •6\.Any Previous History of head and neck radiation therapy
  • •7\.Chemotherapy in the last 12 months
  • •8\.Severe psychologic problems
  • •9\.Failed to sign an informed consent approved by the Human Studies Committee.

Outcomes

Primary Outcomes

Not specified

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