NCT06566001

Brief Summary

22 patient where divided randomly into 2 groups : control group did dental implant utilizing socket shield , while study group did dental implant with allogenic bone graft there is no significant bone loss between the two groups after 4 month follow up

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
22

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 12, 2022

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 20, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 25, 2024

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

August 19, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 22, 2024

Completed
Last Updated

August 22, 2024

Status Verified

March 1, 2022

Enrollment Period

2 years

First QC Date

August 19, 2024

Last Update Submit

August 20, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • measure bone loss by CBCT

    Measure bone loss by CBCT mm

    4 month

Study Arms (2)

control group 11 patients

EXPERIMENTAL

socket shield technique 11 patients

Procedure: control group

study group 11 patients

EXPERIMENTAL

allogenic buccal sheet technique 11 patients

Procedure: control group

Interventions

control groupPROCEDURE

socket shield technique and allogenic bone graft

control group 11 patientsstudy group 11 patients

Eligibility Criteria

Age20 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • \- patient has remaining root in upper anterior without lesion

You may not qualify if:

  • periapical lesion under the tooth

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo university

Giza, Egypt

Location

MeSH Terms

Interventions

Control Groups

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
cairo

Study Record Dates

First Submitted

August 19, 2024

First Posted

August 22, 2024

Study Start

March 12, 2022

Primary Completion

March 20, 2024

Study Completion

May 25, 2024

Last Updated

August 22, 2024

Record last verified: 2022-03

Locations