Immediate Implant Placement With Immediate Professionalization in Aesthetic Area

Implant Site Reaction Clinical Trial

Official title:

Immediate Implant Placement With Immediate Professionalization in the Maxillary Esthetic Zone Using Mixture of Allograft and Xenograft vs Xenografts to Augment the Jumping Gap

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03665025
• Other study ID #: 14422017463550
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 1, 2019
• Est. completion date: January 1, 2019

Study information

• Verified date: September 2018
• Source: Cairo University
• Contact: mohamed hammad, BDS
• Phone: 0096551553531
• Email: dr_nucler[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Immediate implant placement with immediate professionalization in the maxillary esthetic zone using mixture of allograft and xenograft vs xenografts to augment the jumping gap

Description:

Implant placement in fresh extraction sockets in conjunction with appropriate guided bone regeneration has many benefits, which ultimately affect the total treatment plan. The immediate placement of implants provides significant advantages, including fewer surgical procedures, shorter treatment time, and improved esthetics. The goals of osseous replacement are maintenance of contour, elimination of dead space, and reduce postoperative infection, provide good support for dental implant and enhance bony and soft tissue healing. allograft bone has gold standard over other augment techniques including favorable bone quality and minimal bone resorption.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 2
• Est. completion date: January 1, 2019
• Est. primary completion date: January 1, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 60 Years

Eligibility

Inclusion Criteria:

• Adult patients with badly broken teeth in upper esthetic zone indicated for extraction, presence of at least 4 mm of bone beyond the root apex to guarantee implant primary stability, implant placement within the alveoli confines.

• Both sexes.

• No intraoral soft and hard tissue pathology.

• No systemic condition that contraindicate implant placement.

Exclusion Criteria:

• Presence of fenestrations or dehiscence of the residual bony Walls after extraction.

• Heavy smokers more than 20 cigarettes per day .(24)

• Patients with systemic disease that may affect normal healing.

• Psychiatric problems

• Disorders to implant are related to history of radiation therapy to the head and neck neoplasia, or bone augmentation to implant site.

Related Conditions & MeSH terms

• Implant Site Reaction

Intervention

Other:
• immediate implant using mixed allograft and xenograft
immediate implant using mixed allograft and xenograft in anterior area to fill jumping area

Locations

Country	Name	City	State
Kuwait	Mohammed	Kuwait	Q8

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Kuwait, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Crestal bone loss	Will be measured using calliper with scale(1-10mm) for evaluation of crestal bone loss around implant which are the lower values represent a better outcome.	1 year
Secondary	Patient satisfaction	Will be measured using a satisfaction table chart which divided in 4 paraments with scale from 1-4 include( pain-infection-radiography-successful implant ),the number represent (4 excellent-3 very good -2 good-1 bad)	1 year