Faculty of dental medicine for girls
Cairo, Egypt
Completed
NCT Number: NCT06867848
Augmentation of Facial Wall in Defective Fresh Extraction Site for Immediate Implant Placement
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.
Completed
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Notify MeKey information
Age range
18 year–50 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
About this study
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 .
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
laminar bone membrane for labial bone augmentation
Procedureadding 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
Other names: pericardium membrane for labial bone augmentation
Primary outcomes
-
primary stability of implant in Newton centimeter and soft tissue healing
Time frame: one week postoperative
Dental implant ratchet to show implant stability and Pink esthetic score for soft tissue healing measurement
Secondary outcomes
-
labial bone thickness formation in millimeters
Time frame: 6 months postoperative
Cone beam computed tomography to show labial bone thickness
Sponsors and collaborators
Lead sponsor
Nuhayra Ashour Muhammed
Other Gov
Registry information
Important dates
- Study start
- 2022
- Primary completion
- 2024
- Study completion
- 2025
- First posted
- Mar 10, 2025
- Registry last updated
- Sep 4, 2025
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.