Masticatory Performance in Bilateral Balanced Occlusion and Lingualized Occlusion in Complete Denture

NCT ID: NCT06811818

Last Updated: 2025-02-06

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

146 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-07-01

Study Completion Date

2024-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This is a randomized control trial to compare masticatory performance in complete dentures with bilateral balanced occlusion or lingualized occlusion.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This study is a randomized control trial to compare the masticatory efficiency of complete dentures with bilateral balanced occlusion with that of lingualized occlusion . Grouping of participants was carried out. Participants divided into two groups one receiving complete dentures with bilateral balanced occlusion and the other group receiving complete dentures with lingualized occlusion . Each participant provided with 15g of peanuts and instructed to chew until ready to swallow . The chew material than spat into the designated container and participants asked to rinse their mouth with water , with the rinse being collected in the same container . The collected material than sieved through 10-Mesh sieve followed by drying the sieved content on blotting paper for 30 minutes. The dried material subsequently weight with an electric balance with precision of 0.01 grams . Masticatory efficiency assessed through mean weight of chewed peanuts.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Masticatory Performance

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

complete denture with bilateral balanced occlusion

complete denture with bilateral balanced occlusion

Group Type ACTIVE_COMPARATOR

complete denture with bilateral balanced occlusion

Intervention Type OTHER

Participants in this group will be given complete dentures with bilateral balanced occlusion

complete denture with lingualized occlusion

complete denture with lingualized occlusion

Group Type ACTIVE_COMPARATOR

complete denture with lingualized occlusion

Intervention Type OTHER

Participants in this group will be given complete dentures with lingualized occlusion

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

complete denture with bilateral balanced occlusion

Participants in this group will be given complete dentures with bilateral balanced occlusion

Intervention Type OTHER

complete denture with lingualized occlusion

Participants in this group will be given complete dentures with lingualized occlusion

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Participants aged 45-65 years.
2. Both genders included.
3. Edentulous patients requiring complete denture.
4. Patients willing to participate in the study .

Exclusion Criteria

1. Participants not willing to participate in the study.
2. Participants with systemic disease .
3. Participants with neuromuscular disorders .
Minimum Eligible Age

45 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Armed Forces Institute of Dentistry, Pakistan

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Seema Khattak

Dr. Seema Khattak , Principal Investigator and Resident Prosthodontics

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Seema Khattak, BDS

Role: PRINCIPAL_INVESTIGATOR

Armed Forces Institute of Dentistry

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Armed Forces Institute Of Dentistry

Rawalpindi, Punjab Province, Pakistan

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Pakistan

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

masticatory performance

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Complete Lower Dentures on 1 or 2 Implants
NCT02117856 ACTIVE_NOT_RECRUITING NA