CompletedNot Applicable

Assessment of Deproteinized Bovine Bone for Immediate Implants Placement in Maxillary Esthetic Zone.

Egypt16 participantsStarted 2025-01-01

Plain-language summary

: Many of studies have been performed to improve osseointegration and bone density around implants by modifying the implant by adding bone graft or substitute material that increase success of implant. Aim: The aim of this study is to evaluate clinically the efficacy of deproteinized bovine bone in maxillary Esthetic zone to promote bone formation and improve outcomes in immediate implant cases. Methodology: 16 immediate implants will be placed in maxillary esthetic zone. That study will be Conducted on 16 hopeless teeth divided equally and randomly into two groups Randomization will be done using www.randomizer.org ., Group 1: 8 hopeless teeth will be replaced by immediate dental implants represent the (control group) where the implants will be placed without bone graft, Group 2: 8 hopeless teeth will be replaced by immediate dental implants represent the (study group) where the implants will be placed with deproteinized bovine bone graft. The implant stability will be assessed clinically using (Ostell) immediate postoperative and after 6 months and Postoperative pain using visual analogue scale (VAS)

Who can participate

Age range

20 Years – 55 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Patients with hopeless teeth at maxillary esthetic zone.
. Both genders.
. Middle age adults (from 20 years to 55 years).
. The tooth to be extracted had little to no loss of periodontal bone.
. The tooth where endodontic involvement, root fracture, root resorption, periapical pathology, root perforation

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Postoperative Pain (Visual Analog Scale, VAS)

Timeframe: 1, 3, and 7 days postoperatively

Visual Scale of Edema

Timeframe: 1, 3, and 7 days postoperatively

Implant Stability (ISQ)

Timeframe: Baseline (immediately after implant placement) and 6 months postoperatively

Peri-implant Bone Density

Timeframe: Baseline (immediately after implant placement) and 6 months postoperatively

Trial details

NCT IDNCT07569146

SponsorSuez Canal University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-12-05

View on ClinicalTrials.gov More Implant Therapy trials

Plain-language summary

Who can participate

Age range

20 Years – 55 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Patients with hopeless teeth at maxillary esthetic zone.
. Both genders.
. Middle age adults (from 20 years to 55 years).
. The tooth to be extracted had little to no loss of periodontal bone.
. The tooth where endodontic involvement, root fracture, root resorption, periapical pathology, root perforation

What they're measuring

Postoperative Pain (Visual Analog Scale, VAS)

Timeframe: 1, 3, and 7 days postoperatively

Visual Scale of Edema

Timeframe: 1, 3, and 7 days postoperatively

Implant Stability (ISQ)

Timeframe: Baseline (immediately after implant placement) and 6 months postoperatively

Peri-implant Bone Density

Timeframe: Baseline (immediately after implant placement) and 6 months postoperatively