Evaluation for Healing of Iatrogenic Perforation After Repair With Different Materials

NCT ID: NCT06976411

Last Updated: 2025-05-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

PHASE4

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-01

Study Completion Date

2025-12-31

Brief Summary

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The goal of this clinical trial is to evaluate healing potentiality of MTA and bioceramics materials as a root perforation repair material.

The main questions it aims to answer are:

is there is a significant difference in healing potentiality of MTA and bioceramics materials as a root perforation repair material?

Participants will:

enrollment will be from out-patients clinic of endodontic department, faculty of dentistry, Ain Shams university with root perforations. perforation repair will be done using either bio-ceramic or MTA repair material and preoperative or immediate postoperative CBCT and postoperative CBCT will be taken to compare healing.

Detailed Description

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Conditions

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Root Perforation at the Bifurcation Area

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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MTA

Group Type EXPERIMENTAL

MTA

Intervention Type DRUG

Perforation repair using MTA repair material

Bioceramic

Group Type EXPERIMENTAL

Bioceramic putty

Intervention Type DRUG

Perforation repair using Bioceramic repair material

Interventions

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MTA

Perforation repair using MTA repair material

Intervention Type DRUG

Bioceramic putty

Perforation repair using Bioceramic repair material

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Patients with root perforation in lower molars.
2. Patients had anon contributory medical history.
3. Patients of age categories between 15 to 50 years old.
4. No sex restriction.
5. Small to medium size perforation.

Exclusion Criteria

1. Patients with generalized chronic periodontitis.
2. Teeth with difficult isolation.
3. Non restorable teeth.
4. Medically compromised patients.
5. Patients with history of allergies to any of the medications to be used during or after the treatment.
Minimum Eligible Age

15 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ain Shams University

OTHER

Sponsor Role collaborator

Mohamed Salah Elwakeel

OTHER

Sponsor Role lead

Responsible Party

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Mohamed Salah Elwakeel

Assistant lecturer

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Faculty of dentistry ain shams university

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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FDASU-REC 1117 pro

Identifier Type: -

Identifier Source: org_study_id

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