- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05429606
Effect of Different Conductive Media on the Efficacy of Electric Pulp Tester
June 17, 2022 updated by: nosheen sarwar, Pakistan Institute of Medical Sciences
Effect of Different Water-based and Gel-based Conductive Media on the Efficacy of Electric Pulp Tester
Dental pulp tests are investigations that offer valuable diagnostic and treatment planning information to the dental clinician.
EPT is a sensibility test that can be easily performed in clinical practice.
Current study is to find the best conducting substance among readily available water-based gels and gel-based tooth pastes to evaluate the efficacy of electric pulp tester.
Study Overview
Status
Recruiting
Conditions
Detailed Description
The study will be performed on dental students with written informed constant.
The sample size of study is 100.
There will two main groups of conductor materials used in the study: water-based gels (fluoride gel, electrode gel and chlorohexidine gluconate) and gel-based toothpastes (Colgate and Dentonic Ultrawhitening gel).
All groups will be randomly applied to the same patient at a single visit.
Two measurements will be recorded for each material and the average value of the two measurements will used.
Then, the measurements will record, and a comparison will be made between different conductors.
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Islamabad Capital Territory
-
Islamabad, Islamabad Capital Territory, Pakistan
- Recruiting
- School of Dentistry, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad
-
Principal Investigator:
- nosheen sarwar, BDS
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The study subjects are dental students of School of dentistry Islamabad
Description
Inclusion Criteria:
- Healthy fully erupted teeth maxillary central incisors.
- Study subjects above 18 years.
- No systemic diseases and pregnancy
Exclusion Criteria:
- Carious, decayed and periodontally affected teeth.
- Taking anti-inflammatory drugs from last 2 weeks.
- Taking cortisone for the last 6 month
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
---|
Group 1: Fluoride gel
The fluoride gel used as conductive media for electric pulp tester in this group
|
Group 2:Electrode gel
In Group 2 electrode gel applied as conductive media for electric pulp test.
|
Group 3: chlorohexidine gluconate gel
chlorohexidine gluconate gel used as conductive media for electric pulp tester in group 3.
|
Group 4:Colgate gel toothpaste
Colgate gel toothpaste gel used as conductive media for electric pulp tester in group 4.
|
Group 5:Dentonic Ultrawhitening gel
Dentonic Ultrawhitening gel used as a conductive media in Group 5.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Efficacy of electric pulp tester
Time Frame: immediately after procedure
|
To measure the efficacy of electric pulp tester with different conductive media.
|
immediately after procedure
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Effect of gender on efficacy of electric pulp tester.
Time Frame: immediately after procedure
|
To measure the efficacy based of gender in study subjects
|
immediately after procedure
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: nosheen sarwar, BDS, School of dentistry PIMS
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 2, 2022
Primary Completion (Anticipated)
September 1, 2022
Study Completion (Anticipated)
October 1, 2022
Study Registration Dates
First Submitted
June 17, 2022
First Submitted That Met QC Criteria
June 17, 2022
First Posted (Actual)
June 23, 2022
Study Record Updates
Last Update Posted (Actual)
June 23, 2022
Last Update Submitted That Met QC Criteria
June 17, 2022
Last Verified
June 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- SOD/ERB/2022/06
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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