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Destructed Teeth Restored by Zirconia CrownsNCT04875468

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

A study testing TheraCem self-adhesive resin cement and Multilink adhesive resin cement in people with Destructed Teeth Restored by Zirconia Crowns and Zirconia Crowns, run by Diana Mostafa Habeb at 1 site in Egypt.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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… Read more about this study

Who is it for?
Ages 18 to 50 yearsHealthy volunteers can take part
What is being tested?
TheraCem self-adhesive resin cement and Multilink adhesive resin cement
Could I receive a placebo?
No, everyone receives an active treatment
How many people
16 participants
Where
1 siteEgypt
Study dates
May 2021to Jan 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • All subjects are required to be:
  • From 18-50 years old, be able to read and sign the informed consent document.
  • Have no active periodontal or pulpal diseases, have teeth with good restorations
  • Psychologically and physically able to withstand conventional dental procedures
  • Patients with teeth problems indicated for single crowns:
  • Badly decayed teeth
Show all 12Show fewer
  • Teeth restored with large filling restorations
  • Endodontically treated teeth
  • Malformed teeth
  • Malposed teeth (Tilted, over-erupted, rotated, etc.)
  • Spacing between teeth
  • Able to return for follow-up examinations and evaluation.

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Diana Mostafa Habeb, Msc of fixed Prosthodontics contact

+201096643699

diana.mustafa@dentistry.cu.edu.eg

Ashraf Mokhtar, Professor contact

+201001443006

Egypt1 site, 1 recruiting
  • Faculty of Dentistry Cairo University

    Cairo, Giza Governorate, 12613

    Diana Mostafa Habeb, +20109643699, diana.mustafa@dentistry.cu.edu.eg

    Recruiting

Other trials in Egypt

About this study

Official title: Clinical Outcomes of Bonded Monolithic Translucent Zirconia Crowns Using Two Different Compositions of Self-adhesive Resin Cements (Randomized Clinical Trial)

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:

  1. 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:
  5. Badly decayed teeth
  6. Teeth restored with large filling restorations
  7. Endodontically treated teeth
  8. Malformed teeth
  9. Malposed teeth (Tilted, over-erupted, rotated, etc.)
  10. Spacing between teeth
  11. 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)
Being tested
TheraCem self-adhesive resin cement, Multilink adhesive resin cement
Keywords
Marginal adaptation, patient satisfaction
Medical subject headings
Dental Caries, Tooth Discoloration, Patient Satisfaction

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TheraCem self-adhesive resin cementOther

    MDP, calcium and fluoride releasing cement for dental zirconia crowns

  • Multilink adhesive resin cementOther

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

Study groups in NCT04875468
Study groupRoleWhat they receive
Zirconia crown cemented by adhesive resin cementActive comparatorMultiRein link adhesive resin cement (non MDP, non-calcium and fluoride releasing cement)
Receives: Other: Multilink adhesive resin cement
Zirconia crown cemented by self-adhesive resin cementExperimentalTheraCem self-adhesive resin cement (MDP, calcium and fluoride releasing cement)
Receives: Other: TheraCem self-adhesive resin cement

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

    Measured: 9 months

Secondary outcomes (2)
  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

    Measured: 9 months

  2. Patient satisfaction

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

    Measured: 9 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 May 2021
  2. Study startMay 2021 (estimated)
  3. Primary completionJan 2022 (estimated)
  4. Study completionJan 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
16 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04875468
Sponsor's protocol ID
28611222102086
Status last verified
May 2021
First submitted
30 Apr 2021
Last updated
25 May 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing TheraCem self-adhesive resin cement and Multilink adhesive resin cement in people with Destructed Teeth Restored by Zirconia Crowns and Zirconia Crowns, run by Diana Mostafa Habeb at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 12 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 25 May 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Diana Mostafa Habeb, Msc of fixed Prosthodontics (+201096643699, diana.mustafa@dentistry.cu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Marginal discoloration (time frame: 9 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 May 2021.

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