Khyber College of Dentistry
Peshawar, KPK, 25000, Pakistan
Location contact
Asif ullah khan, Associate Professor(Prostho)
CONTACT
Farhad Ali, Assistant Professor
CONTACT
Zainab Rehman, Postgraduate Resident
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07100678
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.
Trial opening soon.
Get Notified18 year–60 year
All sexes
Interventional
Not applicable
Peshawar, KPK, 25000, Pakistan
Asif ullah khan, Associate Professor(Prostho)
CONTACT
Farhad Ali, Assistant Professor
CONTACT
Zainab Rehman, Postgraduate Resident
PRINCIPAL_INVESTIGATOR
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
Time frame: Baseline (before prosthesis placement) and one week after prosthesis delivery.
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.
Contact information is provided by the study sponsor or research team.
Asif ullah Khan, Associate Professor(prostho)
CONTACT
Zainab Rehman, Postgraduate Resident Prostho
CONTACT
Khyber College of dentistry
Other
Comparison Of Pretreatment Expectations and Posttreatment Satisfaction In Patients Receiving Porcelain-Fused-to-Metal Fixed Dental Prosthesis: A Quasi-Experimental Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07737392
Behavior, Health Behavior
Houston, Texas, United States
View Trial DetailsNCT07698041
Behavior, Chronic Pain
Reading, United Kingdom
View Trial DetailsNCT07599358
Anxiety, Anxiety Disorders
View Trial DetailsNCT07416175
Behavior, Health Behavior
View Trial Details