Efficacy of i-PRF Usage in Vestibular Socket Therapy
A Novel Method for Evaluating i-PRF Usage in Vestibular Socket Therapy for Immediate Implant in Defective Fresh Extraction Site
1 other identifier
interventional
24
1 country
1
Brief Summary
This study aims for evaluation of A novel method for evaluating i-PRF usage in vestibular socket therapy for immediate implant in defective fresh extraction site.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2023
Typical duration for not_applicable
1 active site
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
November 21, 2023
CompletedFirst Submitted
Initial submission to the registry
July 31, 2024
CompletedFirst Posted
Study publicly available on registry
December 26, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 21, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 21, 2026
CompletedDecember 26, 2025
December 1, 2025
2.2 years
July 31, 2024
December 12, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
assessment of pink aesthetic score of the gingiva
Assessment of clinical and aesthetic parameters after the newly proposed immediate implant placement technique. using pik aesthetic score of gingiva, The Pink Esthetic Score (PES) is a dental assessment tool scoring gingival aesthetics around implants, evaluating mesial/distal papillae, tissue level/contour/color/texture, and alveolar deficiency. Scoring System 0 (Poor): Marked deficiency or abnormality. 1. (Fair): Slight change or minor discrepancy. 2. (Excellent): Healthy, normal, ideal appearance.
6 and 9 months.
Secondary Outcomes (1)
Facial bone thickness
base line, 6 and 9 months.
Study Arms (2)
deficient facial plate of bone management VST only
EXPERIMENTALSockets with deficient facial plate of bone and intact soft tissue will receive VST only.
deficient facial plate of bone management with VST and iPRF.
ACTIVE COMPARATORSockets with deficient facial plate of bone and intact soft tissue will receive VST and iPRF.
Interventions
Preoperative procedure: cone beam computed tomography (CBCT) scan will be used for diagnosis and treatment planning. Nonsurgical periodontal treatment including scaling and root planning will be performed as needed. Under local anesthesia sulcular incisions will be made, and then hopeless teeth will be extracted atraumatically using periotomes. Socket lavage and curettage will be done thoroughly, and dental implants will be inserted.
Preoperative procedure: cone beam computed tomography (CBCT) scan will be used for diagnosis and treatment planning. Nonsurgical periodontal treatment including scaling and root planning will be performed as needed. Under local anesthesia sulcular incisions will be made, and then hopeless teeth will be extracted atraumatically using periotomes. Socket lavage and curettage will be done thoroughly, and dental implants will be inserted with i-prf.
Eligibility Criteria
You may qualify if:
- Patients has one hopeless tooth in the maxillary anterior region with TYPE II according to Elian classification of sockets (10) and sufficient bone apically and palatally.
- The presence of a natural contralateral tooth for the tooth being replaced.
You may not qualify if:
- Extraction sockets were grade III.
- Acute infection related to hopeless tooth.
- Allergy to any material or medication used in the study.
- Medically compromised patients according to modified Cornell Medical Index.
- Heavy smokers.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
AlAzharU
Cairo, Nasr City, 11371, Egypt
MeSH Terms
Interventions
Study Officials
- PRINCIPAL INVESTIGATOR
abdullah el-shamy, MSC
Al-Azhar University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant lecturer of periodontology
Study Record Dates
First Submitted
July 31, 2024
First Posted
December 26, 2025
Study Start
November 21, 2023
Primary Completion
January 21, 2026
Study Completion
March 21, 2026
Last Updated
December 26, 2025
Record last verified: 2025-12