- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05912725
Conventional Impressions Versus Digital Impression Techniques for Implant Supported Screw Retained Prosthesis
Evaluation of the Accuracy of Conventional and Digital Implant Impression Techniques in Bilateral Distal Extension Cases
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Tanta, Egypt, 3111
- Wafaa youssif El ashry
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All participants have sufficient bone length and width for implant insertion.
- General health of the patients was evaluated by taking a full medical history to ensure that these patients were free from any systemic conditions that would have impaired implant osseointegration
- Good oral hygiene
- Sufficient inter-arch spaces
- The opposing arch was almost dentulous, and any missing teeth were restored using a fixed partial denture.
Exclusion Criteria:
- parafunctional habits
- Heavy smoking
- Those patients with systemic diseases that may influence soft or hard tissue healing.
- Patients with a history of radiation therapy in the head and neck region.
- Patients with a history of radiation therapy in the head and neck region.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Accuracy of Implant impression techniques
Active comparative : digital implant impression Participants underwent intra-oral scanning digital impression Experimental : conventional implant impression Participants underwent conventional impressions And right side of pt mouth received screw retained prosthesis constructed from conventional impression left side received screws retained prosthesis constructed from digital impression |
4 implants were placed , 2 implants in each side of the patient mouth opposite lower second premolar and second molar 4 implants were placed , 2 implants in each side of the patient mouth opposite lower second premolar and second molar |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accuracy of digital and conventional implant impression techniques in partially edentulous patient
Time Frame: 12 months
|
GOM Inspect 2016, Gom GmbH,) that was used to superimpose the Standard tessellation language (STL) datasets of conventional open tray impression technique onto the STL file of the reference (digital implant impression technique) to assess the accuracy and calculate the three-dimensional deviations of scan bodies in color- coding map in micrometers (µm)
|
12 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Wafaa Y El ashry, MSc, Tanta university ,Faculty of Dentistry, Prosthodontics department
- Principal Investigator: Wafaa Y El ashry, Tanta university, Faculty of Dentistry, Prosthodontics department
- Principal Investigator: Wafaa Y El ashry, MSc, Tanta University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- RP-9-20-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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