The Effect of Canal Dryness on the Quality of Obturation

NCT ID: NCT05808062

Last Updated: 2023-08-03

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

COMPLETED

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-01

Study Completion Date

2022-12-31

Brief Summary

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The goal of this clinical trial is to evaluate root canal obturation quality. The questions to answer are

* what is the best protocol for canal dryness before obturation ?
* Is compaction necessary ? Volunteer participants will perform root canal treatment in teeth planned for extraction due to orthodontic reasons

Detailed Description

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Conditions

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Obturation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Total dryness

matching paper points are used till they come out completely dry

Group Type ACTIVE_COMPARATOR

Root canal obturation

Intervention Type PROCEDURE

Root canal dryness

Partial dryness

a single matching cone is inserted in the canal for 3 seconds only.

Group Type ACTIVE_COMPARATOR

Root canal obturation

Intervention Type PROCEDURE

Root canal dryness

Interventions

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Root canal obturation

Root canal dryness

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* healthy males and females (Category: American Society of Anesthesiologists class 1)
* aged 23-25 years
* presenting with sound maxillary premolars (non-carious and not previously restored)
* a radiographically visible root canal outline

Exclusion Criteria

* dental students of any level were not eligible to avoid including vulnerability factors.
* pregnant volunteers
* volunteers with complicating systemic disease (ASA 3-6)
* poor oral hygiene
* periodontal disease (probing depth \>3 mm) related to the tooth
Minimum Eligible Age

23 Years

Maximum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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British University In Egypt

OTHER

Sponsor Role lead

Responsible Party

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shehabeldin saber

Pofessor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Shehabeldin Saber, phD

Role: PRINCIPAL_INVESTIGATOR

Faculty of Dentistry, The British University in Egypt

Locations

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Faculty of Dentistry, The British University in Egypt

Cairo, El-Sherouk, Egypt

Site Status

Countries

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Egypt

References

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Zavattini A, Knight A, Foschi F, Mannocci F. Outcome of Root Canal Treatments Using a New Calcium Silicate Root Canal Sealer: A Non-Randomized Clinical Trial. J Clin Med. 2020 Mar 13;9(3):782. doi: 10.3390/jcm9030782.

Reference Type RESULT
PMID: 32183124 (View on PubMed)

Nawar NN, Elashiry MM, El Banna A, Saber SM, Schafer E. Ex-vivo evaluation of clinically-set hydraulic sealers used with different canal dryness protocols and obturation techniques: a randomized clinical trial. Clin Oral Investig. 2024 Oct 27;28(11):612. doi: 10.1007/s00784-024-06006-5.

Reference Type DERIVED
PMID: 39463194 (View on PubMed)

Other Identifiers

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21-038

Identifier Type: -

Identifier Source: org_study_id

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