This Study Will Assess Whether the Treatment Provided by Dentist is Successful in Meeting the Expectations of Patient by Asking Questions Related to Aesthetics, Chewing Ability, Comfort and Phonetics Before and After Providing Treatment and the Patient Will Tell Through Visual Analog Scale

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorKhyber College of dentistry

About this trial

This study aims to assess patient satisfaction after receiving porcelain-fused-to-metal fixed dental prostheses. Patients will be asked about their expectations before treatment and their satisfaction afterward. The findings will help evaluate whether the treatment meets patient needs and guide improvements in dental care.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Partially edentulous subjects between age group of 18 to 60 years.

Patients who require and are willing to receive a fixed dental prosthesis.

Patients with no experience of Fixed dental prosthesis previously.

Disqualifiers

Patients diagnosed with any psychological disorders (diagnosed by physician).

Patients with facial anomalies like cleft lip and palate.

Patients with skeletal class 2 or class 3.

Patients with facial paralysis, stroke, and speech disorders.

Trial design

Design model

Single group

Treatments tested in this trial

  • Porcelain-Fused-to-Metal Fixed Dental Prosthesis

    Procedure/Surgery

    This prosthesis consists of a metal substructure for strength and a porcelain coating for improved aesthetics. The treatment will be planned and delivered by prosthodontic specialist. The intervention is non-surgical

Treatment groups

120 Participants
are divided into 1 treatment group
Group A: Porcelain-Fused-to-Metal Fixed Dental ProsthesisExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Assessment of Patient Satisfaction Before and After Fixed Prosthodontic Treatment

Patient satisfaction will be assessed in four domains-esthetics, comfort, chewing ability, and phonetics using a 10-point Visual Analogue Scale (VAS). Scores before treatment (expectation) and after treatment (satisfaction) will be compared to determine the change. . Each domain will be scored on a scale from 1 to 10, where 1 represents the lowest level of outcome and 10 represents the highest. The investigator will assess the results by adding all the marked values by the participant on VAS. Minimum and maximum values will be calculated from mean of scores on the basis of data collection results.

Time frame
Baseline (before prosthesis placement) and one week after prosthesis delivery.

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: