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

Bone Resorption Clinical Trial

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04548258
• Other study ID #: 6420
• Status: Recruiting
• Phase: N/A
• Start date: October 2020
• Est. completion date: November 2021

Study information

• Verified date: October 2020
• Source: Cairo University
• Contact: faculty of dentistry cairo university
• Phone: 0235676105
• Email: dentmail[@]dentistry.cu.edu.eg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 12
• Est. completion date: November 2021
• Est. primary completion date: October 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 45 Years to 65 Years

Eligibility

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.

Related Conditions & MeSH terms

• Bone Resorption

Intervention

Device:
• electric intraoral weilding
weilding metal framework to the implants in completely edentulous maxilla using electric weilding device intraorally
• casting
casting metal framework

Locations

Country	Name	City	State
Egypt	Cairo University ,Faculty of Dentistry	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	bony changes assessment	assessment of bone height changes around implants using digital periapical paralling imaging technique and the unit will be meagured in mm.	12 months