NCT05891990

Brief Summary

Evaluation of Soft and Hard Tissue Changes After Immediate Implant Placement With Sticky Tooth Versus Autogenous Tooth Graft for management of Cases With Labial Plate Dehiscence

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2023

Typical duration for not_applicable

Status
unknown

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

First Submitted

Initial submission to the registry

May 27, 2023

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 7, 2023

Completed
4 months until next milestone

Study Start

First participant enrolled

October 1, 2023

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2025

Completed
Last Updated

September 7, 2023

Status Verified

September 1, 2023

Enrollment Period

2.1 years

First QC Date

May 27, 2023

Last Update Submit

September 3, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • Radiographic width of bone labial to the implant

    Amount of bone labial to the implant will be measured perpendicular to the vertical line of the implant surface at the implant neck level or the top of the buccal bone (which is regarded as 0 mm), 3 mm and 6 mm apical to the implant neck Each measurement will be recorded at different times

    1 year

Secondary Outcomes (10)

  • Radiographic horizontal bucco-palatal bone changes

    1 year

  • Radiographic vertical bone changes

    1 year

  • Esthetic evaluation (The pink esthetic score)

    1 year

  • Implant stability

    6 months

  • Gingival Thickness

    1 year

  • +5 more secondary outcomes

Study Arms (2)

Intervention group

EXPERIMENTAL

sticky tooth preparation: * patient's venous blood will be collected using a 21 g needle with a butterfly handle. * The blood in the test tubes will be centrifuged at 700 rpm for 3 min for women and 4 min for men because of a different hematocrit. * The liquid PRF fraction will be collected using a sterile syringe. It gently will be mixed with the demineralized dentin granules and allowed for five-ten minutes for polymerization in order to produce a sticky tooth.

Procedure: immediate implant augmented with sticky tooth

Control group

ACTIVE COMPARATOR

Autogenous demineralized dentin graft preparation * Extracted teeth will be cleaned from periodontal ligaments, cementum, soft tissue attachment, caries, or restorations (if present), using a high-speed fine finishing stone and saline irrigation. * The pulp will be removed, using a root canal instrument. Subsequently, the remaining dentin will be cut into pieces. These pieces of dentin will be ground using a bone mill to produce dentin particles. * The sorted particles will be immersed in 70% ethanol and 4% H2O2 in a sterile container to remove any soft tissue remnants, bacteria, and smear layer. * Tooth particles will be demineralized using 0.6N HCl for 30 minutes to expose the dentine organic matrix. * After demineralization, the materials will be washed with phosphate-buffered saline (PBS) and dried with sterile gauze.

Procedure: immediate implant augmented with autogenous tooth graft

Interventions

* Topical anesthesia will be administered using an infiltration technique. * Atraumatic extraction will be done with the aid of periotome and Luxators. * The extraction socket will be debrided to remove any residual debris or granulation tissue. * Full-thickness midcrestal incision and vertical releasing incision on the distal side will be made, and a vertical releasing incision on the mesial side will be made if necessary. The extraction socket and the labial bone defect will be exposed by buccal and palatal flap reflection. * Implant insertion will be performed according to the manufacturer's instruction, and then the implant will be inserted 2mm apical to the alveolar bone crest with adequate primary stability. * The gap between the implant and the defect of the facial bone will be filled with the sticky tooth to reach enough buccal bone supported and then will be covered with absorbable barrier collagen membranes. * Finally, the flap will be repositioned and sutured.

Intervention group

* Topical anesthesia will be administered using an infiltration technique. * Atraumatic extraction will be done with the aid of periotome and Luxators. * The extraction socket will be debrided to remove any residual debris or granulation tissue. * Full-thickness midcrestal incision and vertical releasing incision on the distal side will be made, and a vertical releasing incision on the mesial side will be made if necessary. The extraction socket and the labial bone defect will be exposed by buccal and palatal flap reflection. * Implant insertion will be performed according to the manufacturer's instruction, and then the implant will be inserted 2mm apical to the alveolar bone crest with adequate primary stability. * The gap between the implant and the defect of the facial bone will be filled with the autogenous demineralized dentin graft to reach enough buccal bone supported and then will be covered with collagen membranes. * Finally, the flap will be repositioned and sutured.

Control group

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Non-restorable teeth in the esthetic zone with a defect of labial bone.
  • Teeth with no acute inflammation.
  • Patients are free from any systemic condition that may affect the healing.
  • Availability of bone apical and palatal to the socket to provide primary stability
  • Good oral health.
  • Willingness to sign the informed consent form.

You may not qualify if:

  • Heavy smoker (\> 10 cigarettes/day)
  • Pregnant females
  • Contraindication for Implant surgery.
  • Patients with poor oral hygiene.
  • Acute inflammation in the site of implantation and adjacent tissue.
  • A history of radiotherapy in the head or neck region.
  • Patients with systemic diseases like uncontrolled diabetes mellitus, coagulation disorders, alcohol or drug abuse not suitable for implantation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Dentist

Study Record Dates

First Submitted

May 27, 2023

First Posted

June 7, 2023

Study Start

October 1, 2023

Primary Completion

October 30, 2025

Study Completion

December 30, 2025

Last Updated

September 7, 2023

Record last verified: 2023-09