Skip to content

Augmentation of Facial Wall in Defective Fresh Extraction Site for Immediate Implant Placement

Augmentation of Facial Wall in Defective Fresh Extraction Site for Immediate Implant Placement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06867848
Enrollment
12
Registered
2025-03-10
Start date
2022-09-15
Completion date
2025-04-01
Last updated
2025-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

the Augmentation of Labial Defective Wall in Fresh Extraction Socket

Keywords

labial bone augmentation, immediate implant placement ., laminar bone membrane effect, pericardium membrane effect

Brief summary

The study is performed to clinically and radiographically assess the efficacy of using enriched bone graft combined with slowly resorbable membrane on bone quality in immediate implant placement in extraction socket in cases with localized facial bone defect.

Detailed description

The study is include twelve participants , and the patients are in rolled in two groups, group one receive implant, sticky bone and laminar bone membrane . group two receive implant, sticky bone and pericardium membrane using vestibular incision and 6 months post operative radiographically assessment is performed to measure labial bone quantity formed .

Interventions

PROCEDURElaminar bone membrane for labial bone augmentation

adding laminar bone membrane in one group and pericardium membrane in another group with sticky bone by using vestibular incision in both groups to augment the labial bone over dental implant

Sponsors

Nuhayra Ashour Muhammed
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

the study is interventional study containing two groups, each group receiving deferent type of treatment for their result comparison.

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* patient with a single hopeless tooth in maxillary anterior region. * sufficient bone apically and palatally * presence of natural contralateral tooth for the tooth being replaced * systemic healthy patients

Exclusion criteria

* extraction socket type III * acute infection in hopeless tooth * a heavy smoker patient * pregnant * had received chemotherapy or radiotherapy in previous year

Design outcomes

Primary

MeasureTime frameDescription
primary stability of implant in Newton centimeter and soft tissue healingone week postoperativeDental implant ratchet to show implant stability and Pink esthetic score for soft tissue healing measurement

Secondary

MeasureTime frameDescription
labial bone thickness formation in millimeters6 months postoperativeCone beam computed tomography to show labial bone thickness

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026