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Molar Incisor HypomineralisationNCT05812690

Molar Incisor Hypomineralisation and Dental Anomalies

An observational study of Molar Incisor Hypomineralisation, run by Sheffield Teaching Hospitals NHS Foundation Trust at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Background/study aim: Molar incisor hypomineralisation (MIH) is a common disorder of tooth development. Affected teeth have weak enamel and adult molars often require extensive treatment or even extraction. Read more about this study

Who is it for?
Ages 7 to 16 yearsHealthy volunteers can take part
Conditions the study is for
Molar Incisor Hypomineralisation
What is being tested?
This is a non intervention - observation only study
How many people
1,279 participants
Where
1 siteUnited Kingdom
Study dates
29 Nov 2022to 22 Aug 2023
Phase
Observational
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 7 to 16 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Study population: The study population is children referred to any of the participating paediatric dentistry clinics for assessment or treatment.

Eligibility criteria Participants are children aged 7-16 years-old, with and without MIH, who meet the inclusion criteria, and attend for assessment or treatment in the participating clinics. To avoid bias, the comparison group will not be solely drawn from a pool of orthodontic patients or those primarily referred with a known diagnosis of dental anomalies

Generic inclusion criteria - all participants (both MIH and comparison groups)

  • No significant medical history (ASA ≤ 2), syndromic conditions, cleft lip and/or palate.
  • Have an existing (full) pan-oral radiograph at recruitment or subsequently undergoes one for routine diagnostic purposes.
  • Child able to accept detailed clinical examination, radiographs (and photographs).
  • Parents and child able to consent/assent to participate in the study and have sufficient level of literacy/understanding to complete written consent forms (with support if necessary).

MIH-group specific inclusion criteria.

  • Children diagnosed with MIH by a specialist in paediatric dentistry according to validated diagnostic criteria (Ghanim et al., 2017, Ghanim et al., 2019) Comparison-group specific inclusion criteria
  • Children referred to the host centre for the management of any dental condition other than MIH.

MIH-group specific exclusion criteria

  • Children with an enamel defect that is not typical of MIH. Comparison-group specific exclusion criteria
  • Children with an atypical pattern of dental caries/extraction in their first permanent molars such that a possible diagnosis of MIH could not be excluded (Ghanim et al., 2017, Ghanim et al., 2019).

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Charles Clifford Dental Hospital

    Sheffield, S Yorks, S10 2TA

Other trials in United Kingdom

About this study

Official title: An International Study of Molar Incisor Hypomineralisation and Its Association With Dental Anomalies

Background/study aim:

Molar incisor hypomineralisation (MIH) is a common disorder of tooth development. Affected teeth have weak enamel and adult molars often require extensive treatment or even extraction. A preliminary study, carried out in Sheffield Dental Hospital, discovered that 12% of MIH children also had congenitally missing adult teeth, presenting further challenges to treatment-planning. This novel finding stimulated discussion between international MIH experts; whilst some clinicians had observed this association, others had not. Therefore the primary aim of this international study is to determine the association between MIH and missing teeth in different populations. This has important clinical and biological relevance in understanding the presentation and management of MIH.

Read more

Participants/research sites:

This study will include 584 children with MIH and a comparison group of 584 children without MIH. Young dental patients, aged 7-16 years, who attend for a check-up or treatment at one of the 15 participating countries will be invited to take part. The UK sites are Sheffield, Newcastle and University College London Dental Hospitals and all children will be seen by specialists/consultants in paediatric dentistry to confirm their diagnosis of MIH. The main inclusion criteria is that children have a dental xray as part of their routine care.

Data collection:

Following a routine dental check-up we will grade the severity of the participants' MIH (if present) and record any other dental anomalies (e.g. abnormal tooth number, position or shape). We will also check the dental xray for other anomalies that cannot be seen from the clinical exam. We will analyse the prevalence of MIH and association with other dental anomalies to see if there are difference according to sex or ethnicity and compare our findings with the non-MIH group. We anticipate the study will take 18 months.

Read the detailed description

The primary objective is to compare the overall prevalence of congenitally missing teeth/hypodontia (excluding wisdom teeth) in children (7-16 years old) with and without MIH.

Secondary research questions/objectives

The secondary research objectives are to:

  1. Compare the prevalence of developmentally missing teeth (hypodontia) in MIH children based on region, ethnicity and gender
  2. Determine the clinical pattern (including symmetry), severity and treatment need of MIH in children (aged 7-16years) referred to specialist paediatric dentistry services across the world, according to gender and ethnic group/region
  3. Compare the prevalence of other co-existing developmental dental anomalies between the two groups
  4. Compare the prevalence of developing third permanent molars between the two groups

What is the scientific justification for the research?

Molar incisor hypomineralisation (MIH) is one of the most common disorders of tooth development seen in paediatric dentistry practice around the world. A recent meta-analysis of 99 studies, in 43 different countries, estimated the global prevalence of MIH to be 13.1% with significant variations seen between super-regions, regions and countries.

A wide variety of other dental anomalies are also seen in childhood, broadly encompassing deviations in tooth number, morphology, structure, position and eruption. Prevalence data for all these different developmental disorders vary widely, depending on the anomaly in question, diagnostic approach and the target population . It is also important to note that the presence of one anomaly should always alert clinicians to the possibility of others, as numerous studies have demonstrated significant inter-relationships between certain anomaly types. Recently, a UK study explored, for the first time, the prevalence of dental anomalies in children diagnosed with MIH. Clinical and radiographic examination of 101 children aged 6-15 years found that, in total, 29% of patients had another dental anomaly in addition to MIH (Walshaw et al., 2020).

There are established guidelines for the management of children with MIH. In some situations, the extraction of one or more first permanent molars is the preferred option, providing all other permanent teeth (and preferably third permanent molars/wisdom teeth) are present. Thus, the congenital absence of a second premolar in the same quadrant would have considerable impact on this decision and potentially compromises long-term outcomes. A controlled study, exploring any association between the presence of MIH and hypodontia, in addition to other dental anomalies, is clearly warranted to better inform patient management. The need for earlier radiographic examination and definitive treatment for hypomineralised first permanent molars would be paramount if such an association is confirmed by the proposed multi-centre international study.

Design and methodology.

This will be a cross-sectional study involving children with MIH and a comparison group of non MIH-affected children.

Burden to research participants Research participants (MIH and comparison group) will not be required to attend any additional visits other than their scheduled check-up or treatment visit. However, their dental check up will take slightly longer than normal (around an extra 5 minutes) as we will be recording in more detail than usual the condition of their enamel (using a validated scoring system of MIH). They will have a dental xray taken as part of their 'routine care' so will not be exposed to unnecessary ionising radiation. They will also be invited to have clinical photographs of their teeth, which may not have been part of their 'routine care'. They will also be verbally asked two (validated) questions about how they rate their own oral health, which is not part of routine care.

Study population

Participants will be recruited from patients attending for treatment, a recall or new patient assessment, in the host centres. Written informed consent will be obtained for study participation from parents/guardians and children. The 'experimental ' group will be children aged 7-16 years referred to specialist paediatric dentistry services for the management of MIH in the following countries:

  1. Nigeria
  2. Australia-2 centres (both Melbourne)
  3. Chile
  4. Egypt
  5. India
  6. Jordan
  7. Netherlands- 2 centres
  8. New Zealand
  9. Qatar
  10. Singapore
  11. South Sudan
  12. United Kingdom- 3 centres (London, Newcastle, Sheffield)
  13. United States of America
  14. United Arab Emirates
  15. Saudi Arabia

A sample size of 1168 children (584 per group) was calculated. In order to achieve this sample size, each centre will aim to recruit 84 participants (42 patients per MIH group and 42 patients per control group).

Examiner training and calibration

Examiner training and calibration will be conducted on-line, using Microsoft Teams, using a set of ten clinical images and radiographs to ensure that there is acceptable intra-and inter-examiner agreement for key parameters under investigation as follows:

  • Use of a validated MIH index to record severity status for first permanent molars;
  • Clinical and radiographic diagnosis of all dental anomalies (abnormal tooth size, position and shape)
  • Presence/absence of developing third permanent molars (wisdom teeth)
  • Degree of taurodontism (this is an abnormal root canal shape) in lower first permanent molars using established criteria/index All clinicians involved in recording these parameters will have to reach acceptable levels of repeatability.

Examination and data collection An electronic data collection 'form' will be developed and piloted prior to commencement of the main study. The following non-identifiable patient and clinical variables will be recorded prior to transfer to a shared electronic dataset using secure processes.

Demographics

  • Age
  • Sex
  • Ethnicity
  • Primary dental diagnosis for both MIH and control participants.
  • Children's global assessment of their own oral health status Radiographic characteristics All participants must have a full panoral (dental) radiograph of good diagnostic quality, taken for 'routine care'. A record will be made of any abnormalities of tooth shape, number and position from the radiographic presentation.

Assessment of taurodontism (abnormal root canal shape) For patients with mature apical development of their first permanent mandibular molars (10 years and over) an objective assessment of taurodontism will be carried out using digital measurements from panoral (dental) radiographs. This will be done according to established protocols; in brief, a diagnosis of taurodontism will be made if the crown/root ratio of the tooth is >1.1 (indicating that the crown pulp shape is abnormally elongated compared to the root length).

Data entry and statistical analysis.

Each unit will be responsible for anonymised electronic data entry for their participants and will send the complete data set securely to the principal investigators for data analysis.

Simple descriptive analysis will be used to present the demographic, clinical and radiographic findings for the MIH and control groups. In addition, statistical tests will be applied to determine:

  • Any significant difference in the prevalence of dental anomalies (notably congenitally missing teeth) between children with and without a diagnosis of MIH and according to gender and ethnicity
  • Any significant difference in the prevalence/degree of taurodontism (abnormal root canal shape) between children with and without a diagnosis of MIH and according to gender and ethnicity
  • Any significant associations between the severity of MIH and presence of developing wisdom teeth, taurodontism and dental anomalies, according to gender and ethnicity
Being tested
This is a non intervention - observation only study
Keywords
Molar Incisor Hypomineralisation, Dental Anomalies, Children, Hypodontia
Medical subject headings
Molar Hypomineralization, Tooth Abnormalities, Anodontia

What participants receive

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

  • This is a non intervention - observation only studyOther

    This is non intervention study

Study groups in NCT05812690
Study groupRoleWhat they receive
Children with molar incisor hypomineralisationChildren referred to the host centres with a clear diagnosis of MIH, as given by a specialist paediatric dentist
Receives: Other: This is a non intervention - observation only study
Children without molar incisor hypomineralisationChildren referred to the host centres with no evidence of MIH
Receives: Other: This is a non intervention - observation only study

What is being measured

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

  1. Prevalence of a dental anomaly in children with and without MIH

    Presence of any dental anomaly (number, shape, eruption disturbance)

    Measured: recruitment until July 2023

Secondary outcomes (1)
  1. Characteristics associated with presence of a dental anomaly in children with MIH

    Secondary outcome measures for this study include the clinical and/or radiographic severity of MIH in relation to participants' gender, ethnicity/country and their global self-reported oral health,

    Measured: recruitment until July 2023

Timeline

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

  1. First posted14 Apr 2023
  2. Study start29 Nov 2022
  3. Primary completion22 Aug 2023
  4. Study completion22 Aug 2023

Resources

More details

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

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
1,279 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05812690
Sponsor's protocol ID
STH21833
Status last verified
Aug 2024
First submitted
31 Mar 2023
Last updated
21 Aug 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: No participant data will be shared outside the core research team

Publications

  • Walshaw EG, Noble F, Conville R, Anne Lawson J, Hasmun N, Rodd H. Molar incisor hypomineralisation and dental anomalies: A random or real association? Int J Paediatr Dent. 2020 May;30(3):342-348. doi: 10.1111/ipd.12601. Epub 2019 Dec 13.

    PubMed 31790155
  • Baccetti T. A controlled study of associated dental anomalies. Angle Orthod. 1998 Jun;68(3):267-74. doi: 10.1043/0003-3219(1998)0682.3.CO;2.

    PubMed 9622764
  • Brook AH. Variables and criteria in prevalence studies of dental anomalies of number, form and size. Community Dent Oral Epidemiol. 1975 Nov;3(6):288-93. doi: 10.1111/j.1600-0528.1975.tb00326.x.

    PubMed 1104248
  • Ghanim A, Silva MJ, Elfrink MEC, Lygidakis NA, Marino RJ, Weerheijm KL, Manton DJ. Molar incisor hypomineralisation (MIH) training manual for clinical field surveys and practice. Eur Arch Paediatr Dent. 2017 Aug;18(4):225-242. doi: 10.1007/s40368-017-0293-9. Epub 2017 Jul 18.

    PubMed 28721667
  • Schwendicke F, Elhennawy K, Reda S, Bekes K, Manton DJ, Krois J. Global burden of molar incisor hypomineralization. J Dent. 2018 Jan;68:10-18. doi: 10.1016/j.jdent.2017.12.002. Epub 2017 Dec 6.

    PubMed 29221956

Questions about this trial

What is this clinical trial studying?

An observational study of Molar Incisor Hypomineralisation, run by Sheffield Teaching Hospitals NHS Foundation Trust at 1 site in United Kingdom.

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

Who may be eligible to take part?

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: finished, as of the sponsor's last update on 21 Aug 2024. 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 United Kingdom. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prevalence of a dental anomaly in children with and without MIH (time frame: recruitment until July 2023). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05812690, which also lists 5 linked publications.

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 21 Aug 2024.

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