Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06642753

Buccal Plate Augmentation Using Sticky Bone Versus Sticky Bone Filling in the Jumping Gap With Immediate Implant Placement in the Maxillary Esthetic Zone: A Randomized Controlled Trial

Led by Cairo University · Updated on 2024-10-23

20

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the pink esthetic score after Buccal Plate Augmentation using Sticky Bone compared to using Sticky Bone as a jumping gap filling material during immediate implant placement in the upper front teeth area. The study includes patients needing extraction of a non-restorable maxillary tooth in the esthetic zone, with intact buccal bone, to assess these two different surgical approaches. Patients will undergo clinical examinations including medical and dental history, periapical radiographs, and cone beam CT scans to evaluate bone and tooth root conditions before surgery. During treatment, venous blood will be collected to prepare platelet-rich fibrin (PRF) components mixed with bone particles to create sticky bone. In the experimental group, sticky bone is placed into a surgical pouch beside the buccal bone plate, while in the control group, sticky bone is used to fill the gap around the implant in the socket. Both groups receive immediate implant placement and healing abutment attachment. Participants will have follow-up visits at 3 and 6 months post-surgery for evaluation. Assessments include pink esthetic scoring, crestal bone level, thickness of the labial bone plate, soft tissue contour, and patient satisfaction. Standardized imaging and clinical exams will be used to monitor healing and implant integration. The total study duration includes these follow-ups to track outcomes and safety.

CONDITIONS

Brief Title

Buccal Plate Augmentation Using Sticky Bone With Simultaneous Immediate Implant Placement

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older
  • Non-restorable maxillary tooth in the esthetic zone (front teeth and premolars) indicated for extraction
  • Intact buccal bone plate after tooth extraction
  • Full-mouth plaque and bleeding score not exceeding 20%
  • Motivation to follow post-operative care and attend follow-up visits
Not Eligible

You will not qualify if you...

  • Periapical infection involving the tooth to be extracted
  • Presence of periodontal disease
  • Systemic health conditions affecting healing such as Diabetes Mellitus or Leukemia
  • Pregnant or nursing females
  • Smokers

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single day procedure

Participants undergo atraumatic tooth extraction, immediate implant placement, and receive sticky bone grafting either in a surgical pouch for buccal plate augmentation or as a filling material in the jumping gap. Blood is drawn to prepare autologous PRF used in the grafting process, followed by placement of a healing abutment on the implant.

1 visit (in-person)

Follow-up

Duration - 6 months

Participants attend follow-up visits to assess healing, esthetic outcomes, crestal bone level, thickness of labial bone plate, soft tissue profile, and patient satisfaction up to 6 months after the implant placement.

Visits at immediately after implant placement, 3 months, and 6 months postoperatively

Trial Site Locations

Total: 1 location

1

Faculty of Dentistry Cairo University

Cairo, Egypt, 12613

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Research Team

Y

Yara KH Ghaith

E

Enji ahmed, Professor

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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