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Modified Periosteal Inhibition With Simultaneous Implant Placement in Aesthetic Zone

StatusCompleted
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Phase changed: Phase 1/2 → not applicable Trial completed · Eligibility criteria expanded, about 11 words · Secondary endpoints: details revised at 3 of 4 entries · 2 more Show 5 more changesShow less
    • Trial completed
    • Eligibility criteria expanded, about 11 words
    • Secondary endpoints: details revised at 3 of 4 entries
    • Study description expanded, about 11 words
    • Site details revised
  2. Secondary endpoints: details revised at 4 of 4 entries Study description revisedv4 Show 1 more changeShow less
    • Study description revised

    See this version in full on ClinicalTrials.gov ↗

  3. Study description expanded, about 20 wordsv3 See this version in full on ClinicalTrials.gov ↗
  4. Re-verified, no change to tracked fieldsv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
A randomized controlled clinical and radiographic trial. Twenty sites with remaining roots or non-restorable teeth in the maxillary anterior region that fulfill the inclusion criteria will be selected from the Periodontology Clinic, Faculty of Dentistry, Tanta University. These sites will be divided into two groups; each of which has ten surgical sites. After phase I therapy, a traumatic extraction of the hopeless tooth will be made trying as much as possible to preserve the labial plate of bone and overlying soft tissue. * Once the tooth is extracted, the socket is gently debrided and irrigated using sterile saline solution. Then the dental implant is placed in the best prosthetic driven position, following the guidelines for immediate implants using prefabricated computer guided surgical template. * After accurate implant placement, a full-thickness flap will be elevated at mesial and distal papilla making a buccal envelope. A bone lamina 0.5 mm thickness will be trimmed and hydrated in sterile saline solution for 30 s to soften it; it should be 1-2 mm larger and deeper than the vestibular bone.
Trial Details
NCT Number NCT06519773
Lead Sponsor Tanta University
Conditions Immediate Dental Implant
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov