Evaluation of Pulp Response to Castor Oil

NCT ID: NCT05723900

Last Updated: 2023-02-13

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

31 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-15

Study Completion Date

2022-12-15

Brief Summary

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The present study was conducted to evaluate and compare pulp response to Castor oil versus Formocresol as Pulpotomy Medicaments in Primary Teeth

Detailed Description

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Conditions

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Pulp Response to Castor Oil

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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Castor oil

Castor oil applied to one side of the selected primary canine

Group Type EXPERIMENTAL

Castor oil

Intervention Type DRUG

Procedure :pulpotomy procedure and histological evaluation. A sample of sixty two primary teeth from thirty healthy cooperative children of both sexes who were between 7-9 years and referred to Pediatric Dentistry Department. Two sound teeth without pulpotomy procedure were extracted and subjected to histological procedures to examine the normal pulp tissue and tissue organization (Negative control). The pulpotomy procedure was performed in sixty primary teeth (by split mouth design).

group I treated with castor oil

Formocresol

Formocresol applied to other side

Group Type EXPERIMENTAL

Formocresol

Intervention Type DRUG

Group II treated with formocresol

Interventions

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Castor oil

Procedure :pulpotomy procedure and histological evaluation. A sample of sixty two primary teeth from thirty healthy cooperative children of both sexes who were between 7-9 years and referred to Pediatric Dentistry Department. Two sound teeth without pulpotomy procedure were extracted and subjected to histological procedures to examine the normal pulp tissue and tissue organization (Negative control). The pulpotomy procedure was performed in sixty primary teeth (by split mouth design).

group I treated with castor oil

Intervention Type DRUG

Formocresol

Group II treated with formocresol

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* healthy cooperative children with sound primary canines indicated for extraction for orthodontic reasons

Exclusion Criteria

* caries primary canines Presence of systemic pathology
Minimum Eligible Age

7 Years

Maximum Eligible Age

9 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Tanta University

OTHER

Sponsor Role lead

Responsible Party

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Shimaa Hadwa

Lecturer in pediatric dentistry department faculty of dentistry tanta university

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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shomaa Mostafa Hadwa, PHD

Role: PRINCIPAL_INVESTIGATOR

Tanta University

Locations

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Faculty of dentistry

Tanta, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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#R-PED-10-22-6,

Identifier Type: -

Identifier Source: org_study_id

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