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Bone Changes Assessment in Screw-Retained Maxillary Complete Denture With Electric Welded Framework Versus Cast One

Bone Changes Assessment in Screw-Retained Maxillary Implant Supported Complete Denture With Electric Welded Metal Framework Versus Cast One (Randomized Control,Split Mouth Trial)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04548258
Enrollment
12
Registered
2020-09-14
Start date
2020-10-31
Completion date
2021-11-30
Last updated
2020-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Resorption

Brief summary

comparing bony changes around implants that will be joined by ametal framework either with electric weiling or with the conventional casting metal

Detailed description

joining multiple implants together in the edentulous arches is considered agood solution, using the conventional casting technique has many disadvantages due to lab errors and time and cost consuming on ,the other hand the study aims to owercome these disadvantages using electric welding metal framework.

Interventions

DEVICEelectric intraoral weilding

weilding metal framework to the implants in completely edentulous maxilla using electric weilding device intraorally

DEVICEcasting

casting metal framework

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
45 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age range from 30 to 65 years old. * Absence of any medical disorder that could complicate the Surgical phase or affect osseointegration. * The patients must be completely edentulous. * The patient must have enough bone height for implants minimum length of 10mm and a minimum diameter of 5 mm. * Patients with good oral hygiene. * Complete denture wearer. * Adequate inter arch space for screw retained prosthesis. * Absence of any intra-oral pathological condition.

Exclusion criteria

Patients with recent extraction(less than three months). * Patients with inflamed ridge or candida infection. * Patients with flappyridge. * Parafunctional habits.

Design outcomes

Primary

MeasureTime frameDescription
bony changes assessment12 monthsassessment of bone height changes around implants using digital periapical paralling imaging technique and the unit will be meagured in mm.

Countries

Egypt

Contacts

Primary Contactfaculty of dentistry cairo university
dentmail@dentistry.cu.edu.eg0235676105

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026