Soft Tissue Graft Versus Acellular Dermal Matrix in Preservation of Buccal Plate of Bone

Comparative Study Clinical Trial

Official title:

Soft Tissue Graft Versus Acellular Dermal Matrix in Preservation of Buccal Plate of Bone After Immediate Implant Placement

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06229561
• Other study ID #: Nmohamed
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: January 18, 2020
• Est. completion date: May 20, 2023

Study information

• Verified date: January 2024
• Source: Faculty of Dental Medicine for Girls
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Comparative study between 2 groups to assess the feasibility of using Acellular dermal matrix vs Soft tissue Graft after immediate implant placement

Description:

It was conclude that SCTG is the gold standard for soft tissue augmentation up till now, However ADM can be alternative to autogenous soft tissue graft.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: May 20, 2023
• Est. primary completion date: November 20, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 50 Years

Eligibility

Inclusion Criteria:

Medically free

Exclusion Criteria:

Heavy smoking

Related Conditions & MeSH terms

• Comparative Study

Intervention

Combination Product:
• Acellular Dermal Matrix
Feasibility of soft tissue graft after immediate implant placement

Locations

Country	Name	City	State
Egypt	Azhar University	Madinat Nasir

Sponsors (1)

Lead Sponsor	Collaborator
Faculty of Dental Medicine for Girls

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Elaskary A, Abdelrahman H, Elfahl B, Elsabagh H, El-Kimary G, Ghallab NA. Immediate Implant Placement in Intact Fresh Extraction Sockets Using Vestibular Socket Therapy Versus Partial Extraction Therapy in the Esthetic Zone: A Randomized Clinical Trial. I — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Buccal bone thickness	Assess the buccal bone thickness before and after the graft application	6 months follow up