NCT07304986

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

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 21, 2023

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

July 31, 2024

Completed
1.4 years until next milestone

First Posted

Study publicly available on registry

December 26, 2025

Completed
26 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 21, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 21, 2026

Completed
Last Updated

December 26, 2025

Status Verified

December 1, 2025

Enrollment Period

2.2 years

First QC Date

July 31, 2024

Last Update Submit

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

EXPERIMENTAL

Sockets with deficient facial plate of bone and intact soft tissue will receive VST only.

Procedure: Immediate implant with VST

deficient facial plate of bone management with VST and iPRF.

ACTIVE COMPARATOR

Sockets with deficient facial plate of bone and intact soft tissue will receive VST and iPRF.

Procedure: Immediate implant with VST and i-prf

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.

deficient facial plate of bone management VST only

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.

deficient facial plate of bone management with VST and iPRF.

Eligibility Criteria

Age15 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

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

Location

MeSH Terms

Interventions

proliferation regulatory factors, human urine

Study Officials

  • abdullah el-shamy, MSC

    Al-Azhar University

    PRINCIPAL INVESTIGATOR

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

Locations