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NCT04324697: Shell grafting

Radiographic and Histological Evaluation of Regenerated Bone After Grafting Using Allograft Shell and Autogenous Chips

Completed Phase 4 Last updated 9 June 2020
What this trial tests

Phase 4 trial testing Horizontal alveolar bone augmentation in Alveolar Bone Resorption in 10 participants. Completed in 5 September 2019.

Timeline
8 April 2018
Primary endpoint
1 July 2019
5 September 2019

Quick facts

Lead sponsorOctober 6 University
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment10
Start date8 April 2018
Primary completion1 July 2019
Estimated completion5 September 2019
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

October 6 University

Who can join

Adults 18 to 50, any sex, with Alveolar Bone Resorption. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The clinical cases in the present study described the khoury shell technique using an allograft plate and autogenous chips, for horizontal reconstruction of the anterior alveolar ridge in the esthetic zone. Without need to use autogenous bone graft techniques that are characterized by more aggressive surgery.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Anterior Aesthetic Zone Reconstruction with Allogenic Bone Shell and Autogenous Bone Chips - An Evaluative Study.
    Karkar KT, Metwally SA, Mohsen KMA. · · 2023 · cited 2× · PMID 37711516 · DOI 10.4103/ams.ams_34_23

Verify or expand the search:

Other recruiting trials for Alveolar Bone Resorption

Currently open trials in the same condition.

Other October 6 University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04324697.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing