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Not yet recruitingNCT07100678Updated Aug 7, 2025

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

An interventional study of Porcelain-Fused-to-Metal Fixed Dental Prosthesis in Patient Satisfaction, sponsored by Khyber College of dentistry. Not yet recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-08-07.

Sponsored by Khyber College of dentistry · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Not applicable
Ages
18 Years to 60 Years
Sex
All
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Study summary

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.

Read the detailed description

This quasi-experimental study is designed to compare pretreatment expectations and posttreatment satisfaction in patients receiving porcelain-fused-to-metal fixed dental prostheses. The study will be conducted at the Prosthodontic Department of Khyber College of Dentistry, Peshawar, over a duration of six months.

A total of 120 partially edentulous patients aged 18 to 60 years, with no prior experience of fixed dental prostheses, will be included using a consecutive non-probability sampling technique. Prior to treatment, participants will be evaluated for their expectations regarding aesthetics, chewing ability, comfort, and phonetics using a validated questionnaire and a Visual Analogue Scale (VAS). Posttreatment satisfaction will be assessed using the same scale-on the day of prosthesis placement for aesthetics and phonetics, and after one week for chewing ability and comfort.

The aim is to evaluate whether there is a significant difference between what patients expect before treatment and how satisfied they are after receiving the prosthesis. The results will also help determine whether factors such as gender or age group influence satisfaction levels. This study seeks to contribute to more patient-centered treatment planning and improved outcomes in prosthodontic care.

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Conditions studied

  • Patient Satisfaction

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Keywords

  • patient satisfaction PFM Prosthodontics
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In context

Patient Satisfaction

256 studies on the registry are indexed under Patient Satisfaction; 127 are open to participants now.

This study's planned enrollment of 120 is above the median of 90 across 196 interventional studies indexed under Patient Satisfaction.

Browse Patient Satisfaction studies →

Lead sponsor

Khyber College of dentistry is the lead sponsor of 5 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 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.

Exclusion criteria

Exclusion Criteria:

  • 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.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Porcelain-Fused-to-Metal Fixed Dental Prosthesis

    Procedure: Porcelain-Fused-to-Metal Fixed Dental Prosthesis

Interventions

  • ProcedurePorcelain-Fused-to-Metal Fixed Dental Prosthesis

    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

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What researchers measure

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.

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Study locations

1 site
  • Khyber College of Dentistry
    Peshawar, KPK 25000, Pakistan
    • Asif ullah khan, Associate Professor(Prostho) · Contact · asif.ullah@kcd.edu.pk · 03018874955
    • Farhad Ali, Assistant Professor · Contact · farhadkcd@gmail.com · 03325925549
    • Zainab Rehman, Postgraduate Resident · Principal investigator
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References and documents

Publications

  • Alqutaibi AY, Alharbi AF, Alharbi AM, Karbouji GA, Dagharire EY, Aboalrejal A. Pretreatment expectations and posttreatment satisfaction with different prosthodontic treatments in a Saudi population. Saudi J Oral Sci. 2022;9(1):63-71. DOI: 10.4103/sjoralsci.sjoralsci_52_21.

Individual participant data

Plan to share: No — IPD will not be shared due to privacy and confidentiality concerns, as well as institutional policies that restrict the dissemination of identifiable health information of study participants.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 7, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07100678
Lead sponsor
Khyber College of dentistry
Responsible party
Zainab Rehman (Postgraduate Resident Prosthodontics, Khyber College of dentistry) — Principal investigator
First posted
Aug 3, 2025
Start date
Oct 1, 2025 (estimated)
Primary completion
Dec 30, 2025 (estimated)
Completion
Mar 30, 2026 (estimated)
Last update
Aug 7, 2025

Study contacts

Zainab Rehman, Postgraduate Resident Prostho
Contact
zainab.rehman13@outlook.com
03424532358
Asif ullah Khan, Associate Professor(prostho)
Contact
asif.ullah@kcd.edu.pk
03018874955
Zainab Rehman, Postgraduate Resident(prostho)
principal investigator · Khyber College of dentistry

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

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