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NCT03397316 Clinical Trial

Evaluation of Marginal Bone Loss After Immediate Implant Placement in Esthetic Zone Without Xenograft.

Bone Loss Clinical Trial

Official title:
Evaluation of Marginal Bone Loss After Immediate Implant Placement in Maxillary Esthetic Zone With and Without Xenograft.

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03397316
Other study ID # AlaaCUImplant
Secondary ID
Status Recruiting
Phase N/A
First received January 1, 2018
Last updated January 13, 2018
Start date July 1, 2017
Est. completion date April 1, 2018

Study information
Verified date January 2018
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Marginal bone loss in immediate implant placement in upper esthetic zone by comparing between non grafting in immediate implant placement with xenograft placement in other side.

the study is to assess the marginal bone loss in the two techniques and compare results between them.

Description:

Marginal bone loss in immediate implant placement in upper esthetic zone by comparing between non grafting in immediate implant placement with xenograft placement in other side.

the study is to assess the marginal bone loss in the two techniques and compare results between them after follow up period of 4 months.

Recruitment information / eligibility
Status Recruiting
Enrollment 8
Est. completion date April 1, 2018
Est. primary completion date March 15, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
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 root apex

Exclusion Criteria:

- presence of fenestrations or dehiscences of the residual bony walls after extraction heavy smokers more than 20 cigarettes per day. systemic diseases that may affect normal healing. psychiatric problems.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• xenograft placement .
immediate implant placement in upper esthetic zone with xenograft placement between residual labial bone and implant surface.

Locations
Country Name City State
Egypt Cairo University Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary marginal bone loss Evaluation of marginal bone loss after Immediate implant placement in maxillary esthetic zone with and without xenograft 4 months
Secondary patient satisfaction measure patient satisfaction by patient satisfaction chart. 4 months
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