Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06529653

Ridge Splitting Using Autogenous Bone Wedge Versus the Conventional Intercortical Augmentation Technique in Horizontally Deficient Anterior Maxilla

The current study aimed to evaluate both the quality and quantity of gained and maintained bone width after ridge splitting utilizing autogenic bone wedges versus mixed bone particles for horizontal ridge augmentation in the anterior esthetic zone.

Recruiting

Interested in participating?

Request Info

Key information

Age range

25 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

oral and maxillo facial Surgery Department; Faculty of dentistry, Cairo University.

Cairo, Egypt

Location status: Recruiting

Location contact

yasmin ahmed, B.D.S

CONTACT

01065273456

About this study

This randomized clinical study included 20 patients with a horizontally deficient ridge in the esthetic region. Two groups were divided according to the type of intercortical bone graft used after ridge splitting: 10 patients for each. (The intervention group) had grafting with autogenous bone wedges harvested from the chin, and (the control group) had mixed (autogenic and xenogenic) bone particles.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients possessed partially edentulous anterior maxillary ridge with the following criteria
  • The anterior maxillary vertical dimension was more than ten mm measured from the alveolar crest to the basal bone of the maxilla.
  • The horizontal alveolar dimension varies from 3-5 mm at the crest and 6-8 mm at the basal part of the ridge measured from the labial cortex to the lingual cortex.
  • All patients were free from any medical conditions that may affect bone healing .
  • No local pathosis that may interfere with bone healing.
  • No previous grafting procedures at the indicated edentulous ridge.

-

Exclusion criteria

1- Patients suffering from any systemic disease that may affect bone healing. 2- Patients with less than 3mm labio palatal alveolar ridge width. 3- Ridge with inadequate vertical bone height. 4- Presence of any local pathosis that may interfere with bone healing. 5- Patients unable to continue the whole follow up.

-

Treatment and study plan

autogenous bone wedge

Procedure

autogenous bone block harvested from chin and adjusted to be wedged intercortical in split ridge

Primary outcomes

  1. bone width in (mm) by cone beam pre, immediate post operative and 6 months postoperative

    Time frame: 6 months

    after ridge augmentation in both groups, the bone width will be measured immediately postoperatively and 6 months postoperatively with cone beam and the measurements of the three intervals (pre-, immediate and 6 months postoperatively) will be compared in both groups to evaluate the amount of gained and maintained bone width

Secondary outcomes

  1. percentage of areas of new bone (%)

    Time frame: 6 months

    The harvested core biopsies would be stained with H&E and Massons trichrome stain and be microscopically examined to determine percentage areas of newly formed bone

Study contacts

Contact information is provided by the study sponsor or research team.

Mohamed Omara, PHD

CONTACT

01144452862

yasmin ahmed, B.D.S

CONTACT

[email protected]

01065273456

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Ridge Splitting Using Autogenous Bone Wedge Versus the Conventional Intercortical Augmentation Technique in Horizontally Deficient Anterior Maxilla A Randomized Clinical Trial

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Jul 31, 2024
Registry last updated
Jul 31, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.