Postoperative Pain Assessment After Using Different Kinematics

NCT ID: NCT04277520

Last Updated: 2021-07-27

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

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-02-01

Study Completion Date

2021-07-01

Brief Summary

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The aim of this study is to evaluate postoperative pain after endodontic instrumentation using rotation, reciprocation and adaptive motion.

Detailed Description

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Post operative pain assessment is done at the end of the session Visual Analog Scale (VAS) questionnaires were handed out to the patients and they were asked to assign a number correlating to their post-treatment pain, with 0 representing no pain and 10 representing the most severe pain imaginable.These scores were marked in intervals of 6, 12, 24, 48 and 72 h following endodontic treatment.

Conditions

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Root Canal Therapy

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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Continous rotation

instrumentation was done in continuous rotation motion

Group Type ACTIVE_COMPARATOR

Root canal therapy

Intervention Type PROCEDURE

Different types of instrumentation motions during root canal therapy

Reciprocation

instrumentation was done in reciprocation motion

Group Type ACTIVE_COMPARATOR

Root canal therapy

Intervention Type PROCEDURE

Different types of instrumentation motions during root canal therapy

Adaptive motion

instrumentation was done in adaptive motion

Group Type ACTIVE_COMPARATOR

Root canal therapy

Intervention Type PROCEDURE

Different types of instrumentation motions during root canal therapy

Interventions

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Root canal therapy

Different types of instrumentation motions during root canal therapy

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Medically free patients with good health.
2. Patient's age between 18\_50
3. Mandibular first molars teeth diagnosed clinically and radiographically as acute irreversible pulpitis with no evidence of apical pathosis
4. Positive patient's acceptance for participation in the study

Exclusion Criteria

* Root resorption
* Non restorable teeth.
* Pregnancy.
* Systematic disease as hypertension ,diabetes .
* Psychologically disturbance.
* Need for prophylactic antibiotics
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

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Mohamed Mokhtar Nagy

Associate professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ahmed Hashem, PhD

Role: STUDY_DIRECTOR

Faculty of Dentistry, Ain Shams university

Locations

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Faculty of Dentistry, Ainshams University

Cairo, , Egypt

Site Status

Countries

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Egypt

References

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Gambarini G, Testarelli L, De Luca M, Milana V, Plotino G, Grande NM, Rubini AG, Al Sudani D, Sannino G. The influence of three different instrumentation techniques on the incidence of postoperative pain after endodontic treatment. Ann Stomatol (Roma). 2013 Mar 20;4(1):152-5. doi: 10.11138/ads.0152. Print 2013 Jan.

Reference Type BACKGROUND
PMID: 23741536 (View on PubMed)

Other Identifiers

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ASFD-ENDO-1

Identifier Type: -

Identifier Source: org_study_id

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