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Compares treatment options for Scan Time
Official title Scan Time and Prosthetic Complications of Intraoral Scanning Versus Intraoral Photogrammetry for Full-Arch Titanium Framework With Zirconia Overlay Implant Screw-Retained Prostheses
ClinicalTrials.gov ID: NCT07446790
What this study is testing
- What it's testing
- This study aims to evaluate the effect of intra-oral scanning and intra-oral photogrammetry on scan time and prosthetic complications in patients receiving full-arch titanium framework with zirconium overlay implant screw-retained prostheses. Participants will: Receive a full arch implant prosthesis and scan time will be recorded.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Adults
You may be able to join if
- Patients requiring maxillary and/or mandibular full arch screw-retained implant-supported prosthesis.
- Number of implants placed per arch ranging from 4-6 implants per arch.
- Completely edentulous patients with sufficient inter-arch space to receive fixed prosthesis (Crown height space 9-15 mm per arch).
- Adequate zone of keratinized mucosa (\> 2mm width).
- Both genders.
You likely can't join if
- Completely edentulous patients with insufficient inter-arch space to receive fixed prosthesis (Crown height space lesser than 9mm per arch).
- Completely edentulous patients with in-adequate zone of keratinized mucosa (\< 2mm).
- Un cooperative patients.
- Poor oral hygiene.
- Uncontrolled systemic diseases (Diabetes, hypertension).
See the full eligibility criteria
- Patients requiring maxillary and/or mandibular full arch screw-retained implant-supported prosthesis.
- Number of implants placed per arch ranging from 4-6 implants per arch.
- Completely edentulous patients with sufficient inter-arch space to receive fixed prosthesis (Crown height space 9-15 mm per arch).
- Adequate zone of keratinized mucosa (\> 2mm width).
- Both genders.
- Acceptable oral hygiene.
- Cooperative patients.
- Controlled systemic diseases (Diabetes, hypertension).
- Completely edentulous patients with insufficient inter-arch space to receive fixed prosthesis (Crown height space lesser than 9mm per arch).
- Completely edentulous patients with in-adequate zone of keratinized mucosa (\< 2mm).
- Un cooperative patients.
- Poor oral hygiene.
- Uncontrolled systemic diseases (Diabetes, hypertension).
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, not specified. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.