ClinicalTrials.gg
Not yet recruitingNCT07142746PCTUpdated Aug 27, 2025

Proximal Contact Tightness of Zirconia Crowns: Digital Intraoral Scanning vs Conventional Impressions

An interventional study of Digital intra oral scanning and Conventional impression in Proximal Contacts and Zirconia Crowns, sponsored by Armed Forces Institute of Dentistry, Pakistan. Not yet recruiting at 1 site in Pakistan. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-08-27.

Sponsored by Armed Forces Institute of Dentistry, Pakistan · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Jun 2026, 5 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

We will be comparing the proximal contacts of zirconia crowns and adjacent natural teeth in two groups. One receiving crowns fabricated via digital intra oral scanning means. And the other group recieving crowns fabricated via the dental impression method using trays and impression material.

Read the detailed description

Subjects will be randomly assigned in two groups using a computer generated randomization list. Allocated subjects in groups will be concealed in an envelope. All clinical procedures of crown preparation and cementation will be performed by a single clinician with standard crown preparation guidelines to minimize variability. After standardized tooth preparation for full coverage ceramic crowns, one group will receive conventional impressions using polyvinyl siloxane (PVS) material in trays and other group will be scanned using intra oral digital scanner. Crowns for both groups will be fabricated in the same dental laboratory under standardized conditions.

Proximal and occlusal adjustments will be performed in the oral cavity before cementation at try in and crowns will be cemented using the same luting agent, GIC. After cementation proximal contact tightness will be assessed for the crowns by the digital force gauge at mesial and distal contacts and recorded for data compilation. The 0.05mm metal strip is inserted between the prosthesis and the adjacent natural tooth. The frictional force generated while removing the metal strip slowly in the buccal direction will be recorded on the screen of the customized digital force gauge. The frictional force generated will be considered equal to the proximal contact tightness and will be recorded in Newton (N). Proximal contact tightness will be recorded immediately after the crowns were cemented and at a recall after 10 days. These proximal contact tightness will be compared to see if there lies a significant difference in between the crowns fabricated from both impression techniques.

02

Conditions studied

  • Proximal Contacts
  • Zirconia Crowns
03

In context

Lead sponsor

Armed Forces Institute of Dentistry, Pakistan is the lead sponsor of 27 studies on the registry; 10 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients seeking definitive full coverage ceramic crowns for molars.
  • Patients in age group of 18- 47 years.
  • Patients with healthy adjacent and opposing teeth.
  • Patients with healthy periodontium.

Exclusion criteria

Exclusion Criteria:

  • Patients with grade 1 mobility in adjacent or opposing teeth.
  • Patients with diastema in posterior teeth.
  • Patients having severe malocclusion associated with traumatic occlusion.
  • Patients with temporomandibular joint disorders.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Triple (Care provider, Investigator, Outcomes assessor)
Enrollment
75 participants (estimated)

Study arms

  • Active comparator
    Conventional impression

    One group will be receiving the impression for zirconia crowns by trays and conventional impression material.

    Procedure: Conventional impression

  • Experimental
    Digital Intra Oral Scanning

    One group will recieve digital intra oral scan for obtaining digital scan of anatomy of prepared teeth.

    Procedure: Digital intra oral scanning

Interventions

  • ProcedureDigital intra oral scanning

    One groups prepared teeth will be scanned by a digital intra oral scanner.

  • ProcedureConventional impression

    One group will recieve impressions conventionally in a tray with dental impression polyvinly siloxane.

06

What researchers measure

Primary outcomes

  1. Proximal contact tightness in terms of frictional force generated as shown on digital dynamometre in newtons at cementation day 1.

    Proximal contact tightness will be assesed when shimstock will be pulled out by a hook attached to a digital dynamometre. The frictional force generated in newtons will be assesed and noted at the day 1 of cementation.

    Time frame: Day 1 at cementation of crown.

Secondary outcomes

  1. Proximal contact tightness of zirconia crowns in terms of frictional force in newtons as shown on digital dynamometre at the day 10.

    We will assess the proximal contact tightness of zirconia crowns with adjacent teeth as we pull shimstock with a hook attached to digital dynamometre and asses the frictional force generated in Newtons at the day 10 of cementation of crown.

    Time frame: At 10 days after receiving the treatment crown

07

Study locations

1 site
  • Afid Rawalpindi
    Rawalpindi, Punjab Province 36000, Pakistan
    • Aleeha Dr Aleeha Zahoor Resgistrar prosthodontics, BDS · Contactaleehazahoor10@gmail.com · +923365003656
    • Dr Aleeha Zahoor Dr Aleeha Zahoor Registrar Prosthodontics, BDS · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 27, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07142746
Lead sponsor
Armed Forces Institute of Dentistry, Pakistan
Responsible party
Seema Khattak (REGISTRAR PROSTHODONTICS, Armed Forces Institute of Dentistry, Pakistan) — Principal investigator
First posted
Aug 27, 2025
Start date
Aug 2025 (estimated)
Primary completion
Jun 2026 (estimated)
Completion
Jul 2026 (estimated)
Last update
Aug 27, 2025

Study contacts

Aleeha Dr Aleeha Zahoor, BDS
Contact
aleehazahoor10@gmail.com
+923365003656
Dr Aleeha Zahoor Registrar Prosthodontics
principal investigator · Armed Forces Institute of Rawalpindi

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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