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Effect of Digital Versus Static Jaw Relation Record on Crestal Bone Changes Around Implants Supporting Maxillary Single Overdenture

A

Ain Shams University

Status

Completed

Conditions

Edentulous Jaw

Treatments

Procedure: Maxillary implant supported overdenture , Digital jaw relation group
Procedure: Maxillary implant supported overdenture , Static jaw relation group

Study type

Interventional

Funder types

Other

Identifiers

NCT06965517
FDASU-RecID022140

Details and patient eligibility

About

patients will be equally and randomly divided into 2 groups. Each group contains seven patients: Digital Group: implant supported maxillary overdenture will be constructed using electronic facebow to record maxillo-mandibular relation.

Static Group: implant supported maxillary overdenture will be constructed using the conventional jaw relation method.

Radiographic evaluation for crestal bone height around implants using direct digital periapical paralleling cone technique.

All data of radiographic evaluation were collected and tabulated then statistically analyzed using SPSS software.

Full description

  • Conventional single upper denture will be made for all patients.
  • Occlusal adjustment of lower teeth for all patients by T-scan using the single upper conventional denture.
  • The single maxillary denture will be duplicated with radiopaque markers and CBCT will be used to determine the exact positions of the implants.

Surgical procedures

  1. Surgery will be done under local anesthesia.
  2. Drilling will be carried out under copious sterile irrigation.
  3. four implants will be inserted in canines and second premolar area in the maxilla.

After 3-4 months of implants placement, patients will be equally and randomly divided into 2 groups. Each group contains seven patients:

Digital group: For this group, implant supported maxillary overdenture will be constructed using electronic facebow to record maxillo-mandibular relation.

Static group: For this group, implant supported maxillary overdenture will be constructed using the conventional jaw relation method.

Post insertion:

  • Clinical evaluation for any signs of inflammation is made.
  • Further occlusal refining of lower teeth by T-scan is done with final overdenture.

Method of evaluation:

Radiographic evaluation for crestal bone height around implants using direct digital periapical paralleling cone technique.

All data of radiographic evaluation were collected and tabulated then statistically analyzed using SPSS software.

Enrollment

14 patients

Sex

All

Ages

35 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age: under 60 years.
  • Completely edentulous maxillary arch.
  • Opposing natural dentition in the mandibular arch.
  • Residual mandibular ridge has adequate bone and covered by firm healthy mucosa.
  • Class I maxillary-mandibular relationship.
  • Normal salivary flow with normal viscosity.
  • Systemically free patients.

Exclusion criteria

  • Patients with poor oral hygiene.
  • Patients with abnormal oral habits as (bruxism, clenching, tongue thrusting).
  • Bone or mucosal diseases.
  • Metabolic diseases or uncontrolled diabetes and TMJ disorders.
  • Conditions that may complicate the treatment like; large tongue, gagging reflex and limited mouth opening.
  • Patients who are smokers.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

14 participants in 2 patient groups, including a placebo group

Digital group
Active Comparator group
Description:
implant supported maxillary overdenture constructed using electronic facebow to record maxillo-mandibular relation.
Treatment:
Procedure: Maxillary implant supported overdenture , Digital jaw relation group
Static group
Placebo Comparator group
Description:
implant supported maxillary overdenture constructed using the conventional jaw relation method
Treatment:
Procedure: Maxillary implant supported overdenture , Static jaw relation group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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