NCT07764640

Brief Summary

This in vivo crossover study aims to compare the accuracy of three different final impression techniques for severely resorbed mandibular ridges in completely edentulous patients. The accuracy of the impressions will be evaluated digitally using three-dimensional scanning and deviation analysis to determine differences among the impression techniques.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
8

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Dec 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 12, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 23, 2025

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

June 14, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 10, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 14, 2026

Completed
Last Updated

August 14, 2026

Status Verified

August 1, 2026

Enrollment Period

5 months

First QC Date

August 10, 2026

Last Update Submit

August 12, 2026

Conditions

Keywords

Resorbed ridge,digital analysis,final impression,geomagic

Outcome Measures

Primary Outcomes (1)

  • 3D deviation (RMS) between final impression scans

    The accuracy of the final impression techniques was assessed by three-dimensional deviation analysis of the impression scans using Geomagic Control software. Root Mean Square (RMS) deviation was calculated by comparing the scans obtained using the different impression techniques.

    Immediately after each final impression was recorded

Study Arms (3)

Convensional final impression

EXPERIMENTAL

Conventional final impression technique using alginate impression material followed by zinc oxide eugenol (ZOE) impression material.

Procedure: Conventional final impression

Wax impression technique

EXPERIMENTAL

Wax impression technique using a wax impression followed by alginate impression material.

Procedure: Wax impression technique

compound impression technique

EXPERIMENTAL

Wash compound impression technique using a low-fusing impression compound wash followed by alginate impression material.

Procedure: Compound impression technique

Interventions

Conventional final impression technique using alginate impression material followed by zinc oxide eugenol (ZOE) impression material

Convensional final impression

Wax impression technique using a wax impression followed by alginate impression material.

Wax impression technique

Compound impression technique using a low fusing impression compound followed by alginate impression material.

compound impression technique

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may not qualify if:

  • Completely edentulous patients with severely resorbed mandibular ridges.
  • Patients requiring a mandibular complete denture.
  • Patients able to tolerate the impression procedures and attend the required study visits.
  • Patients willing to participate in the study and provide informed consent.
  • Patients with systemic or local conditions that contraindicate conventional dental impression procedures.
  • Patients with pathological lesions or significant abnormalities affecting the mandibular denture-bearing area.
  • Patients unable to tolerate or cooperate with the impression procedures.
  • Patients who decline to participate or withdraw their informed consent. -

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Dentistry, Tanta University

Tanta, Gharbia Governorate, Egypt

Location

Study Officials

  • Nashwa Ali Saleh, PHD

    Tanta University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of Prosthodontics

Study Record Dates

First Submitted

August 10, 2026

First Posted

August 14, 2026

Study Start

December 12, 2024

Primary Completion

May 23, 2025

Study Completion

June 14, 2026

Last Updated

August 14, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared with other researchers. Only aggregated study results will be reported.

Locations