- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06067945
Comparison of Marginal Fit and Internal Adaptation in All-Metal Crowns: an in Vitro Experimental Trial
February 24, 2025 updated by: Tooba Shabbir, Altamash Institute of Dental Medicine
The goal of this in vitro study is to compare the marginal fit and internal adaptation of all-metal crowns in polished crown preparations and non-polished crown preparations The main question it aims to answer is: are the non polished tooth preparations comparable to polished preparations?
We will compare polish and non polish groups and see their effects on marginal fit and internal adaptation of all metal crown
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
28
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Tooba Shabbir, FCPS
- Phone Number: 03442105654
- Email: tooba.shabbir92@gmai.com
Study Locations
-
-
Sindh
-
Karachi, Sindh, Pakistan, 5444
- Recruiting
- Altamash institute of dental medicine
-
Contact:
- Tooba Shabbir, FCPS
- Phone Number: 03442105654
- Email: tooba.shabbir92@gmail.com
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The phantom teeth (Nissin dental products Inc.
Kyoto 601-8469,Japan) will be fixed in the model plaster block type II (Super national, Karachi Pakistan) with full crown and only 2mm of root portion
Description
Inclusion Criteria:
- Phantom teeth
- Maxillary molars
- Metal crowns with conventional lost-wax technique for crown fabrication
Exclusion Criteria:
- Over prepared or underprepared crowns
- Defective metal crowns
- Ruptured silicone films upon removal
- Defective die stone casts
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
NP is given to the non polished group which is group 2
Out of two groups, group 2 is a test group to which rough preparations are assigned
|
prevention of microleakage and secondary carries
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
marginal fit
Time Frame: six months
|
The margins of fixed restorations refers to the junction between the prepared tooth structure and the crown restoration
|
six months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Internal fit
Time Frame: six months
|
Internal fit is defined as the perpendicular distance between the framework and abutment teeth and the misfit is measured from occlusal/incisal and axial surfaces to the coping
|
six months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Naseer Ahmad, Ph.D, Altamash institute of dental medicine
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)
February 24, 2025
Primary Completion (Estimated)
June 20, 2025
Study Completion (Estimated)
June 20, 2025
Study Registration Dates
First Submitted
September 25, 2023
First Submitted That Met QC Criteria
October 3, 2023
First Posted (Actual)
October 5, 2023
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 24, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- Tshabbir92 Altamash
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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