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NCT05261334 Clinical Trial

Socket Shield Technique Versus Early Implant Placement With Contour Augmentation

Bone Loss Clinical Trial

Official title:
Socket Shielding in Immediate Versus Early Implant Placement With Contour Augmentation of Fresh Extraction Sockets in the Esthetic Zone. A Randomized Pilot Clinical Study.

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05261334
Other study ID # sst versus contour aug
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 31, 2022
Est. completion date September 1, 2023

Study information
Verified date March 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

comparing socket shield technique with early implant placement with contour augmentation in preserving the bone contour

Description:

comparing immediate implant placement with socket shield technique and final crown after 3 months with extraction and after 4 to 8 weeks implant placement with contour bone augmentation then after 3 to 4 months final crown delivery

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 20
Est. completion date September 1, 2023
Est. primary completion date March 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: 1. Non-restorable maxillary teeth in the esthetic zone 2. Intact adjacent teeth 3. Adequate palatal and apical bone that allows achieving implant primary stability. 4. Type I socket 5. =18 years 6. = 60 years 7. Systemically healthy patients Exclusion Criteria: 1. Extraction sockets with acute or chronic infection or with adjacent infected teeth 2. Heavy Smokers > than 10 cigarettes daily 3. Cancer patients undergoing radiotherapy or chemotherapy during or within the last 6 months. 4. Unmotivated patients to maintain adequate oral hygiene to follow up. 5. Patients with physical disabilities that could affect follow up.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• contour augmentation
early implant placement with contour bone augmentation

Locations
Country Name City State
Egypt Cairo University Cairo

Sponsors (1)
Lead Sponsor Collaborator
Iman Abd-ElWahab Radi, PhD

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary facial bone thickness using superimposed CBCT images 12 months
Secondary facial bone height changes using superimposed CBCT images 12 months
Secondary Soft tissue height changes using superimposed intraoral scans 12 months
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