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CAD/CAM Space MaintainerNCT05134714

"Evaluation of Clinical Performance and Success Rate of CAD/CAM Versus Conventional Band and Loop Space Maintainer"

A study testing CAD/CAM zircon band and loop space maintainer and Conventional metal band and loop space maintainer in people with CAD/CAM Space Maintainer, run by Ain Shams University.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

This study is to evaluate and compare CAD/CAM zircon space maintainer and conventional metal of band and loop space maintainers in terms of plaque deposits and gingival health and, the success rate of the appliances in terms of: survival time, cement loss and appliance breakage. Read more about this study

Who is it for?
Ages 4 to 7 yearsHealthy volunteers can take part
Conditions the study is for
CAD/CAM Space Maintainer
What is being tested?
CAD/CAM zircon band and loop space maintainer and Conventional metal band and loop space maintainer
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
18 participants
Where
No sites listed yet
Study dates
1 Jun 2024to 1 Dec 2024
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 4 to 7 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Patients aged :
  • A-minimum:4years B-maximum: 7 years old
  • Patients who are medically free
  • Premature loss of bilateral primary molar.
  • Sound and healthy buccal and lingual surfaces of selected primary molars.

Who cannot join

  • Children with dental abnormalities (cross bite, open bite, and deep bite).
  • Parafunctional oral habits.
  • Carious lingual and buccal surfaces of primary molars.
  • Lack of patient/parent compliance and cooperation.

Trial locations and contacts

No sites are listed yet.

Sara A. Younes, MS contact

00201009334057

sarayounes87@gmail.com

About this study

Official title: "Evaluation of Clinical Performance and Success Rate of CAD/CAM Versus Conventional Band and Loop Space Maintainer Randomized Clinical Trial and in Vitro Study"

This study is to evaluate and compare CAD/CAM zircon space maintainer and conventional metal of band and loop space maintainers in terms of plaque deposits and gingival health and, the success rate of the appliances in terms of: survival time, cement loss and appliance breakage. And to compare both appliances in terms of patient satisfaction.

This study consists of two parts: in vivo part (split mouth RCT) and in vitro part:

Read more

In vivo study:

Its sample size was found to be (36) cases (i.e. 18 case per group). Sample size calculation was performed using G*Power version 3.1.9.7 Sample size will be increased by about 10% to compensate for the drop-out.

In this in vivo study split mouth will be randomly divided into two groups:

Group 1: Conventional metal band and loop space maintainer Group 2: CAD/CAM zircon band and loop space maintainer

In vitro study:

its sample size was found to be (24) samples (i.e. 8 samples per group). Sample size calculation was performed using G*Power version 3.1.9.7 Sample size will be increased by about 10% to compensate for the drop-out.

Grouping:

The zirconia specimen divided randomly into three groups according to type of cements:

Group 1: Self-adhesive resin cement Group 2: Resin-modified glass ionomer cement Group 3: Universal bioactive cement

Read the detailed description

Introduction:

Primary teeth play an important role in the development and growth of a child. Although their role in esthetics, speech, eating, and to encourage normal function. The other main function of a primary tooth is to hold space for the permanent successor until it's time for eruption. This normal physiologic process can be affected due to early premature loss of primary molars, due to dental caries which may lead to mesial tipping or migration of large permanent molar teeth into the space created. This may result in loss of space leading to discrepancy of arch length, malocclusion, crowding of teeth, cross bite, impaction of permanent premolars, and supra-eruption of opposing tooth. The best approach to maintain arch space and to prevent malocclusion is to use a space maintainer. Band and loop has been used since long as a space maintainer with high success rates. But there are some disadvantages can be associated with space maintainers which include, loss of cement, solder failure, caries formation along the margins of the band, long construction time, and the possibility of metal allergy in some patients. These shortcomings in addition to the rising interest of esthetic dentistry augmented by advances in technology have led to the development of newer materials and designs in the fabrication of space maintainers such as fiber-reinforced composite resins (FRCR) as fixed space maintainers. Digital technologies such as CAD CAM technology and new materials are becoming popular, getting better and changing the way to therapy. The ceramic space maintainer seems to be a suitable alternative to the conventional band and loop space maintainer. The appliance is well tolerated by the patient and also gives the benefit of advanced aesthetics with improved strength and allowing the easiest way of debonding during eruption of permanent successors.

The aim of the current study is:

  1. Primary Objective Evaluate and compare CAD/CAM zircon space maintainer and conventional metal of band and loop space maintainers in terms of plaque deposits (Plaque index), gingival health (Gingival index).

The success rate of appliances in terms of survival time, cement loss and appliance breakage.

  1. Secondary Objectives Compare both appliances in terms of patient satisfaction. Evaluate the shear bond strength of three different cements used for CAD CAM zircon space maintainer cementation in vitro.

This study consists of two parts: in vivo part (split mouth RCT) and in vitro part:

1- In vivo study:

Study design:

A split mouth Randomized controlled clinical trial (RCT)

In this in vivo study split mouth will be randomly divided into two groups:

Group 1(study group): CAD/CAM zircon band and loop space maintainer Group 2(control): Conventional metal band and loop space maintainer Interventions

All interventions will be performed by the primary investigator as follows:

Control group:

  1. Stainless steel appropriate band will be selected according to the size of the abutment teeth.
  2. Then the band will be seated on the tooth and full arch impression will be obtained using alginate material.
  3. The band will be removed gently and then stabilize in the impression material.
  4. Maxillary impression will be obtained using alginate material.
  5. Impressions will be poured in stones and then design of the loop will be obtained, then will be send to the laboratory for soldering.
  6. Afterwards abutment teeth will be cleaned.
  7. Isolations precautions will be taken.
  8. Cementing the space maintainer using glass ionomer cement.
  9. Any excess material will be removed. Study group
  10. Impression of the upper and lower arches will be taken using elastomeric impression material.
  11. Impressions will be send to the lab for fabrication of zircon space maintainer.
  12. Solid monolithic zirconia material which utilizes CAD/CAM technology for its designing and milling of the restoration will be used for fabrication of the space maintainer.
  13. Lab Procedure: zircon CAD/CAM-fabricated material has to be digitally designed by a technician using a digital scanner and design software.
  14. CAD CAM space maintainer will be cemented. Oral hygiene instructions will be given to patients as a standard of care after dental procedures.

Clinical evaluation Clinical evaluation of success rates of the modalities regarding survival time, cement loss, breakage of the appliances.

Plaque index, that is running in a scale from 0 to 3 where 0 means no plaque,1 film of plaque adhering to free gingival margin,2 moderate accumulation of soft deposits on the tooth and gingival margin, and 3 means abundance of soft debris (according to the PI described by Silness \& Loe) Gingival health, scores from 0 to 3 where 0 no inflammation, 1slight redness no bleeding on probing, 2 redness and bleeding on probing, and 3 severe inflammation with edema and ulceration to spontaneous bleeding (according to the GI described by Silness \& Loe), and patient satisfaction (checked using visual analogue scale (six point facial Wong-Baker Scale) in vivo.

Follow up and outcome:

Patients will be recalled for clinical follow up after 3, 6, 9 and 12 months. 2- In vitro study:

Materials:

Three different cements, namely, self-adhesive resin cement, resin-modified glass ionomer cement, and universal bioactive cement, will be used in this study. All of the materials will be applied according to the manufacturers' instructions.

Grouping:

The zirconia specimen divided randomly into three groups according to type of cements:

Group A: Self-adhesive resin cement Group B: Resin-modified glass ionomer cement Group C: Universal bioactive cement

Specimen collection and Preparation for shear bond strength:

Freshly extracted human molars, caries free will be collected and examined by stereomicroscope to exclude any specimen with cracks.

The roots of each tooth will be removed, the teeth will be cleaned and polished with non-fluoridated flour of pumice for 10s using rubber cup, and then rinsed with stream of water and then drying it.

Teeth will be mounted in a self-cure acrylic resin so that the crown will be exposed, the acrylic blocks will be number coded with a different number for each group of samples.

Preparation of zirconia specimens Zirconia specimens will be milled from yttrium-stabilized tetragonal zirconia (Y-TZP). The bonding site of each specimen will be finished using 600-, 800-, 1000- and 1200-grit silicon carbide paper to obtain a flat surface. All the zirconia specimen will be ultrasonically cleaned in deionized water for 5 min and divided into three groups according to the types of cements.

Cementation protocol The zirconia specimens will be divided into three groups according to type of cement.

The zirconia specimens will be bonded to the enamel specimen of the extracted teeth by cement prepared according to the manufacturer's instructions. Excess cement was removed.

Specimens will be held in a fixed position without any movement for 5 min to achieve self-curing without motion.

Shear Bond Strength testing After the cementation procedure, all specimens will be stored at 37°C in distilled water for 24 h. Then, the specimens will be subjected to Shear Bond Strength testing by applying a shear load to the zirconia until bond failure occurred.

Following deboning, the specimen will be examined under a stereomicroscope to determine the mode of bond failures (adhesive, cohesive, or mixed).

Being tested
CAD/CAM zircon band and loop space maintainer, Conventional metal band and loop space maintainer
Keywords
space maintainer, CAD/CAM space maintainer

What participants receive

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

  • CAD/CAM zircon band and loop space maintainerDevice

    Also called CAD/CAM space maintainer

    Solid monolithic zirconia material which utilizes CAD/CAM technology for its designing and milling of the restoration will be used for fabrication of the space maintainer.

  • Conventional metal band and loop space maintainerDevice

    Also called metal band and loop space maintainer

    Stainless steel appropriate band will be selected according to the size of the abutment teeth and then design of the loop will be obtained, then will be send to the laboratory for soldering.

Study groups in NCT05134714
Study groupRoleWhat they receive
Group 1(study group): CAD/CAM zircon band and loop space maintainerExperimentalSolid monolithic zirconia material which utilizes CAD/CAM technology for its designing and milling of the restoration will be used for fabrication of the space maintainer.
Receives: Device: CAD/CAM zircon band and loop space maintainer; Device: Conventional metal band and loop space maintainer
Group 2(control): Conventional metal band and loop space maintainerActive comparatorStainless steel band and loop space maintainer will be made. Stainless steel appropriate band will be selected according to the size of the abutment teeth then design of the loop will be obtained, then will be send to the laboratory for soldering.
Receives: Device: CAD/CAM zircon band and loop space maintainer; Device: Conventional metal band and loop space maintainer

What is being measured

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

  1. Clinical success: Evaluate and compare CAD/CAM zircon space maintainer and conventional metal of band and loop space maintainers in terms of plaque deposits (Plaque index)

    Plaque index, that is running in a scale from 0 to 3 where 0 means no plaque,1 film of plaque adhering to free gingival margin,2 moderate accumulation of soft deposits on the tooth and gingival margin, and 3 means abundance of soft debris.

    Measured: Up to 12 months

  2. Clinical success: Evaluate and compare CAD/CAM zircon space maintainer and conventional metal of band and loop space maintainers in terms of Gingival health, by assessing the gingival index.

    Gingival health, scores from 0 to 3 where 0 no inflammation, 1slight redness no bleeding on probing, 2 redness and bleeding on probing, and 3 severe inflammation with edema and ulceration to spontaneous bleeding,47 and patient satisfaction.

    Measured: up to 12 months

  3. The success rate of appliances in terms of survival time.

    Clinical evaluation of success rates of the modalities regarding survival time by checking both space maintainers and identify if there is cement loss or breakage of the appliances during the follow up period.

    Measured: Up to 12 months

Secondary outcomes (1)
  1. Compare both appliances in terms of patient satisfaction.

    patient satisfaction by (checked using visual analogue scale )patients will be choose from smiley faces if they are happy or not

    Measured: Up to 12 months

Timeline

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

  1. First posted26 Nov 2021
  2. Study start1 Jun 2024 (estimated)
  3. Primary completion1 Nov 2024 (estimated)
  4. Study completion1 Dec 2024 (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
Model description
Assignment
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
18 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05134714
Sponsor's protocol ID
PED 21-4D
Status last verified
Jan 2024
First submitted
2 Nov 2021
Last updated
31 Jan 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing CAD/CAM zircon band and loop space maintainer and Conventional metal band and loop space maintainer in people with CAD/CAM Space Maintainer, run by Ain Shams University.

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 5 inclusion and 4 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 31 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.

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 Sara A. Younes, MS (00201009334057, sarayounes87@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Clinical success: Evaluate and compare CAD/CAM zircon space maintainer and conventional metal of band and loop space maintainers in terms of plaque deposits (Plaque index) (time frame: Up to 12 months). The study lists 3 primary outcomes in all. 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 31 Jan 2024.

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