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Status unknownNCT04875468Updated May 25, 2021

Clinical Outcomes of Bonded Monolithic Translucent Zirconia Crowns Using Two Different Compositions of Self-adhesive Resin Cements

An interventional study of TheraCem self-adhesive resin cement and Multilink adhesive resin cement in Destructed Teeth Restored by Zirconia Crowns, Zirconia Crowns and Decayed, Missing, and Filled Teeth, sponsored by Diana Mostafa Habeb. Status unknown at 1 site in Egypt. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-05-25.

Sponsored by Diana Mostafa Habeb · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified May 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

The aim of the present study is to evaluate the clinical outcomes (marginal discoloration, marginal adaptation, gingival health, debonding and patient satisfaction) of translucent zirconia crowns bonded by TheraCem (MDP, calcium and fluoride releasing) self-adhesive resin cement compared to multilink self-adhesive resin cement.

Read the detailed description

Clinical outcomes of bonded monolithic translucent zirconia crowns using two different compositions of self-adhesive resin cements (Randomized Clinical Trial)

Research question:

Will TheraCem self-adhesive resin cement (MDP, calcium and fluoride releasing cement) give better outcomes when bonding monolithic translucent zirconia crowns to tooth structure compared to Multilink self-adhesive resin cement (non MDP, non-calcium and fluoride releasing cement) in terms of marginal discoloration, marginal adaptation, gingival health, debonding and patient satisfaction?

PICOS:

P: Population: Patients requiring single zirconia crowns I: Intervention: TheraCem self-adhesive resin cement (MDP, calcium and fluoride releasing cement) C: Comparison: Multilink adhesive resin cement (non MDP, non-calcium and fluoride releasing cement)

O: Outcomes:

Outcomes Primary outcome Marginal discoloration using USPHS for 9 months Secondary outcomes 1. Marginal adaptation

  1. patient satisfaction

Statement of the problem:

Bonding of zirconia restorations to tooth structures is still challenging. The success of the restoration may be affected by the type of cement used as it may affect marginal discoloration, marginal adaptation, gingival health, debonding and patient satisfaction. The effect of newly introduced TheraCem self-adhesive resin cement (MDP, calcium and fluoride releasing cement) on the clinical behavior of bonded translucent monolithic zirconia is not yet fully reported.

Aim of the study:

  • The aim of the present study is to evaluate the clinical outcomes (marginal discoloration, marginal adaptation and patient satisfaction) of translucent zirconia crowns bonded by TheraCem (MDP, calcium and fluoride releasing) self-adhesive resin cement compared to multilink self-adhesive resin cement.

Research null hypothesis:

-There will be no difference in color stability, marginal adaptation and patient satisfaction of translucent zirconia crowns bonded either with TheraCem or Multilink self-adhesive resin cements.

Primary objective:

The Primary outcome: Marginal discoloration using USPHS Secondary outcomes: 1. Marginal adaptation 2. Patient satisfaction

Trial design:

Parallel group, two arms, with 1:1 ratio

Methods:

A) Participants, interventions, and outcomes

Study setting: This study will be carried out on patients enrolled from the Outpatient clinic in fixed prosthodontics clinic, Faculty of Dentistry, Cairo University.

Eligibility criteria:

Inclusion criteria:

All subjects are required to be:

  1. From 18-50 years old, be able to read and sign the informed consent document.
  2. Have no active periodontal or pulpal diseases, have teeth with good restorations
  3. Psychologically and physically able to withstand conventional dental procedures
  4. Patients with teeth problems indicated for single crowns:

    1. Badly decayed teeth
    2. Teeth restored with large filling restorations
    3. Endodontically treated teeth
    4. Malformed teeth
    5. Malposed teeth (Tilted, over-erupted, rotated, etc.)
    6. Spacing between teeth
  5. Able to return for follow-up examinations and evaluation.

Exclusion criteria:

  1. Patient less than 18 or more than 50 years
  2. Patient with active resistant periodontal disease
  3. Patients with poor oral hygiene and uncooperative patients
  4. Pregnant women
  5. Patients in the growth stage with partially erupted teeth
  6. Psychiatric problems or unrealistic expectations

Interventions:

TheraCem (MDP containing - calcium and fluoride releasing self-adhesive resin cement).

Outcomes The outcomes will be assessed at the following time points

T0 = immediately after restoration delivery

Primary Marginal Discoloration Alpha (A): no discoloration (There is no visual evidence of marginal discoloration different from the color of the restorative material and from the color of the adjacement.

(visual inspection)

Bravo (B): discoloration without axial penetration (There is visual evidence of marginal discoloration at the junction of the tooth structure and the restoration, but the discoloration has not penetrated along the restoration in a pulpal direction.

(visual inspection)

Charlie (C): discoloration with axial penetration (There is visual evidence of marginal discoloration at the junction of the tooth structure and the restoration that has penetrated along the restoration in a pulpal direction. (visual inspection Secondary 1.Marginal Adaptation Alpha (A) No visible evidences of crevice along the margins; no catch or penetration of the explorer.

Bravo (B) Visible evidence of crevice and/or catch of explorer; no penetration of the explorer.

Charlie (C) Visible evidence of crevice and penetration of explorer 2.Patient satisfaction Numerical (discrete) ("0" unsatisfied - "10" satisfied)

Participant timeline:

  • The patient will be treated in visits designated as follows:

Visit 1: Pre-operative records, face-to-face adherence reminder session, clinical, radiographic examination, intraoral photographs and primary impression (alginate impression*) for diagnostic cast construction.

Visit 2: Teeth preparation, secondary impression using addition silicone rubber base material† and temporary restoration‡.

Visit 3: Try in Visit 4: placement and permanent cementation of the final restoration.

* Marginal discoloration, color stability, marginal adaptation and patient satisfaction will be evaluated immediately after cementation.

Recall visits:

The same evaluators evaluated the participants during the recall appointments with a mirror and a sharp explorer at 3 months, 6 months, and 9 months. Periapical radiographs were made and postoperative data were collected and used as a documentation tool with the clinical photographs. Marginal adaptation, esthetics, patient satisfaction and clinical examination were assessed using USPH After delivering the crowns, the participants were asked to rate the level of the satisfaction with their restorations by using a 1 to 10 numeric rating scale (1=poor, 5=acceptable, 10=excellent) at 3 months, 6 months and 9 months. Mean, standard deviation and 95% confidence interval for the mean were used to summarize patient satisfaction.

Data collection methods:

Primary outcome: Marginal discoloration will be assessed by using HSPHS criteria Secondary outcomes: 1. Marginal adaptation will be assessed using the modified USPHS criteria.

  1. Patient satisfaction will be assessed by using normal scores numerical score from 1 to 10 (1=poor, 5=acceptable, 10=excellent)
02

Conditions studied

  • Destructed Teeth Restored by Zirconia Crowns
  • Zirconia Crowns
  • Decayed, Missing, and Filled Teeth
  • Tooth Discoloration

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Keywords

  • Marginal adaptation, patient satisfaction
03

In context

Tooth Discoloration

102 studies on the registry are indexed under Tooth Discoloration; 19 are open to participants now.

This study's planned enrollment of 16 is below the median of 48 across 95 interventional studies indexed under Tooth Discoloration.

Browse Tooth Discoloration studies →

Lead sponsor

This is the only study on the registry with Diana Mostafa Habeb as lead sponsor.

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

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • All subjects are required to be:

    1. From 18-50 years old, be able to read and sign the informed consent document.
    2. Have no active periodontal or pulpal diseases, have teeth with good restorations
    3. Psychologically and physically able to withstand conventional dental procedures
    4. Patients with teeth problems indicated for single crowns:

      1. Badly decayed teeth
      2. Teeth restored with large filling restorations
      3. Endodontically treated teeth
      4. Malformed teeth
      5. Malposed teeth (Tilted, over-erupted, rotated, etc.)
      6. Spacing between teeth
    5. Able to return for follow-up examinations and evaluation.

Exclusion criteria

Exclusion Criteria:

    1. Patient less than 18 or more than 50 years 2. Patient with active resistant periodontal disease 3. Patients with poor oral hygiene and uncooperative patients 4. Pregnant women 5. Patients in the growth stage with partially erupted teeth 6. Psychiatric problems or unrealistic expectations
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
16 participants (estimated)

Study arms

  • Active comparator
    Zirconia crown cemented by adhesive resin cement

    MultiRein link adhesive resin cement (non MDP, non-calcium and fluoride releasing cement)

    Other: Multilink adhesive resin cement

  • Experimental
    Zirconia crown cemented by self-adhesive resin cement

    TheraCem self-adhesive resin cement (MDP, calcium and fluoride releasing cement)

    Other: TheraCem self-adhesive resin cement

Interventions

  • OtherTheraCem self-adhesive resin cement

    MDP, calcium and fluoride releasing cement for dental zirconia crowns

  • OtherMultilink adhesive resin cement

    (non MDP, non-calcium and fluoride releasing cement)

06

What researchers measure

Primary outcomes

  1. Marginal discoloration

    Alpha (A): no discoloration (There is no visual evidence of marginal discoloration different from the color of the restorative material and from the color of the adjacement. (visual inspection) Bravo (B): discoloration without axial penetration (There is visual evidence of marginal discoloration at the junction of the tooth structure and the restoration, but the discoloration has not penetrated along the restoration in a pulpal direction. (visual inspection) Charlie (C): discoloration with axial penetration (There is visual evidence of marginal discoloration at the junction of the tooth structure and the restoration that has penetrated along the restoration in a pulpal direction. (visual inspection

    Time frame: 9 months

Secondary outcomes

  1. Marginal Adaptation

    Alpha (A) No visible evidences of crevice along the margins; no catch or penetration of the explorer. Bravo (B) Visible evidence of crevice and/or catch of explorer; no penetration of the explorer. Charlie (C) Visible evidence of crevice and penetration of explorer

    Time frame: 9 months

  2. Patient satisfaction

    Numerical (discrete) ("0" unsatisfied - "10" satisfied)

    Time frame: 9 months

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 25, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04875468
Lead sponsor
Diana Mostafa Habeb
Responsible party
Diana Mostafa Habeb (Assistant Lecturer of Fixed Prosthodontics, Cairo University) — Sponsor-investigator
First posted
May 6, 2021
Start date
May 2021 (estimated)
Primary completion
Jan 2022 (estimated)
Completion
Jan 2022 (estimated)
Last update
May 25, 2021

Study contacts

Diana Mostafa Habeb, Msc of fixed Prosthodontics
Contact
diana.mustafa@dentistry.cu.edu.eg
+201096643699
Ashraf Mokhtar, Professor
Contact
+201001443006

Oversight

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

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