- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05153213
Correlation of Length of Index Finger to Vertical Dimensions of Occlusion for Edentulous Patients
December 9, 2021 updated by: Shujah Adil Khan, Dow University of Health Sciences
Correlation of Length of Index Finger to Vertical Dimensions of Occlusion for Edentulous Patients and Assessment of Patient Satisfaction - A Randomized Clinical Trial
This study is a randomized clinical trial comparing the conventional method of recording occlusal vertical dimension using Willis gauge from the base of the nose to the base of the chin with the other method using vernier caliper for the length of the index finger to access the satisfaction level of edentulous patients acquiring complete dentures.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study was to apply the anthropometric methods to correlate the length of fingers to occlusal vertical dimensions and also by using the Willis Method to assess the occlusal vertical dimension for edentulous patients and assess satisfaction by comparing both the methods for patients who are in the process of acquiring complete dentures.
Furthermore, conventional methods are applied most commonly for the recording of occlusal vertical dimensions.
This study also bridged the knowledge gap among clinicians to adapt to a different methodology for recording the VDO using the anthropometric measurement of fingers which would improve denture satisfaction.
Therefore, a total of 71 patients were selected for this study, having lost their OVD due to the complete absence of teeth and having no history of maxillofacial or orthognathic surgery, nor any skeletal deformities or disfigurement of fingers.
The measurements were made at the appointment for jaw relations records in which the length of the fingers was measured with a digital Vernier caliper and also the conventional methods were applied for recording the occluding vertical dimensions which included recording the distance from the base of the nose septum (Subnasion - Sn) to the base of the chin (Menton - Me) (Sn-Me).
The length of the index finger (2D) was recorded and a correlation was found between Sn-Me and finger length.
Study Type
Interventional
Enrollment (Actual)
71
Phase
- Not Applicable
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
-
-
Sindh
-
Karachi, Sindh, Pakistan
- Dow University of Health Sciences
-
-
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
30 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Completely edentulous patients
- Patients willing to participate in the study
- Male patients without a beard
Exclusion Criteria:
- Partially dentate patients
- Patients having any maxillofacial or myofascial disorders
- Any history of orthognathic or orthodontic surgery
- Deformities or disfigurement of fingers
- Patients with neurological problems in the head and neck
- Any bony defects or visible sharp spicules
- Nose or chin deformity
- TMJ disorders (intracapsular/extracapsular)
- Heavy bulky chin area (double chin)
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Finger Lengths
Vernier caliper was used to determine the length of Index Finger to record Vertical Dimensions of Occlusion
|
Vernier caliper was used to measure finger length
|
|
Active Comparator: Conventional method
Willis gauge was used to determine the Length from Base of the nose to Base of the chin to record Vertical Dimensions of Occlusion
|
Gillis gauge was used to measure occlusal vertical dimension
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Satisfaction with Complete Dentures
Time Frame: 6 Months
|
Satisfaction with Complete Dentures after assessment of occlusal vertical dimension with Length of Index Finger
|
6 Months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Shujah A Khan, BDS, Dow University of Health Sciences
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
March 1, 2019
Primary Completion (Actual)
July 1, 2019
Study Completion (Actual)
March 1, 2020
Study Registration Dates
First Submitted
March 23, 2021
First Submitted That Met QC Criteria
December 9, 2021
First Posted (Actual)
December 10, 2021
Study Record Updates
Last Update Posted (Actual)
December 10, 2021
Last Update Submitted That Met QC Criteria
December 9, 2021
Last Verified
December 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SAKhanDowUHS
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
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.
Clinical Trials on Patient Satisfaction
-
Shaukat Khanum Memorial Cancer Hospital & Research...CompletedSatisfaction, Patient | SatisfactionPakistan
-
Duke UniversityCompletedPatient Satisfaction | Clinician SatisfactionUnited States
-
Universitair Ziekenhuis BrusselWithdrawnPatient Satisfaction | Patient PreferenceBelgium
-
Cedars-Sinai Medical CenterTerminated
-
HaEmek Medical Center, IsraelUnknownPatient Satisfaction | Patient Compliance
-
Methodist Health SystemCompletedSatisfaction, PatientUnited States
-
Acibadem UniversityCompletedPatient Satisfaction | Patient Relations, NurseTurkey
-
University Hospital, ToulouseCompletedSatisfaction, PatientFrance
-
University of AarhusAarhus University HospitalCompletedPatient Satisfaction | Patient-Centered CareDenmark
-
Dr Abdurrahman Yurtaslan Ankara Oncology Training...CompletedPatient Satisfaction | Bowel Preparation | Patient ExperienceTurkey
Clinical Trials on Finger lengths
-
University of California, IrvineCompleted
-
Centre Hospitalier Departemental VendeeCompletedNutritive ValueFrance
-
Endeavor HealthCompletedHypermobility of Interphalangeal Joints | Swan-Neck DeformityUnited States
-
Loewenstein HospitalTechnion, Israel Institute of TechnologyRecruiting
-
Ataturk UniversityNot yet recruiting
-
Biruni UniversityCompleted
-
University of California, IrvineEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsActive, not recruitingStroke, Ischemic | Cerebrovascular Accident (CVA)United States
-
Amasya UniversityMustela FoundationEnrolling by invitation
-
Hospital Privado de Comunidad de Mar del PlataCompleted