Caries; InitialRIDCBWNCT04092296
Efficacy of Resin Infiltration of Proximal Caries
A study testing resin infiltration and remineralization in people with Caries; Initial, run by Wuhan University at 1 site in China.
Trial summary
The aim of the present study was to assess the clinical efficacy of resin infiltration of interproximal caries lesions using a novel measure method-----DIAGNOcam. This study is conducted on adults (15-40y)with the aim of comparing the therapeutic effects of infiltrating caries lesions and fluoride remineralization… Read more about this study
- Who is it for?
- Ages 15 to 40 yearsHealthy volunteers can take part
- Conditions the study is for
- Caries; Initial
- What is being tested?
- resin infiltration and remineralization
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 37 participants
- Where
- 1 siteChina
- Study dates
- 10 Aug 2018to 10 Aug 2021
- 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 15 to 40 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- individuals who want to participate in the study ,the presence of 2 or more non-cavitated interproximal caries lesions with dark shadow involved in the enamel on the DIAGNOcam image -
Who cannot join
- patient who diagnosed with dentinogenesis imperfecta
Trial locations and contacts
1 site in 1 country.
China1 site, 1 recruiting
- Recruiting
Wuhan university
Wuhan, Hubei
fei wang, graduate, 15927529467, 121565382@qq.com
liuyan meng, doctor, 15827652404, mengliuyan@whu.edu.cn
About this study
Official title: Efficacy of Resin Infiltration of Proximal Caries Tested With DIAGNOcam and Bitewing Radiography:Randomized Controlled Clinical Trial
The aim of the present study was to assess the clinical efficacy of resin infiltration of interproximal caries lesions using a novel measure method-----DIAGNOcam. This study is conducted on adults (15-40y)with the aim of comparing the therapeutic effects of infiltrating caries lesions and fluoride remineralization treatment after 1, 2, and 3 yrs. The outcome (lesion progression) is evaluated by DIAGNOcam and radiographic techniques.And we would compare the sensitivity of monitoring progression of caries between DIAGNOcam and bitewing radiography.
Read the detailed description
On the baseline,At a screening visit, eligibility of interested participants is checked with DIAGNOcam by a researcher(WF),in addition,a pair of standardized conventional bitewing radiographs is taken using a film holder Kwik-Bite by a very experienced dental assistant .
two reviewers(SC、XYJ) who are trained the scoring systems score the DIAGNOcam and bitewing image independently,disagreements are solved by consensus and a final DIAGNOcam and bitewing score are given.Participants who have two E2 lesions are picked to join the first set up.
A.DIAGNOcam image scoring system:
E1:Dark shadow confined to the out half of the enamel E2:Dark shadow confined to the inner half of the enamel D1:Dark shadow reach dentin ,dentin caries penetrating the enamel-dentin junction linerly D2:Deep dentin are involved
B .bitewing radiograph scoring system:
E1 = radiolucency in the out half of the enamel; E2 = radiolucency extending to the enamel dentine junction; D1= radiolucency into dentine but limited to the outer third; D2 = radiolucency into middle or middle third of the dentine; D3 = radiolucency into middle or inner third of the dentine; 2.3 Caries risk and periodontal condition assessment On the baseline ,we use the dmft/s to asess the caries risk.In addition,Occurrence of plaque is scored as 0 = no visible plaque or 1 = visible plaque; the status of the gingiva is scored as 0 = sound, 1 = redness, with no bleeding after probing, 2 = bleeding after probing, and 3 = heavily inflamed.
2.4 Allocation From each pair, 1 lesion is allocated to the "test" and 1 to the "control" group using random number table and sealed in opaque envelope to prevent the allocation being known in advance of, or during, enrolment 2.5 Treatment INTERVENTION 1:Resin infiltration:Treatment is performed by a single trained investigator (WF) at the Wuhan University stomatological Hospital . A rubber dam is applied to achieve dry working conditions. In the test group, allocated teeth are slightly separated by plastic wedges (Wedge Wands, small or medium; Garrison, Übach-Palenberg, Germany) that have been flattened by a scalpel to leave space below the contact point. A piece of polyurethane foil is placed in the contact area with a plastic holder to protect the adjacent tooth. A 15% HCl etching gel (Icon product, DMG, Hamburg,Germany) is applied by syringe in the area below the contact point for 120 sec. Subsequently, the gel is washed off with air-water-spray for 30 sec. The lesion is desiccated by air-blowing for 30 sec, application of ethanol for 30 sec, and air- blow ing again for 30 sec. An infiltrant (Icon product,DMG) is applied with another plastic holder,in this time the investigator need to shut off the light.. After 3 min of penetration time, excess material is removed by air blowing and flossing, and the resin is light-cured for 1 min from the buccal, occlusal, and oral aspects. The infiltration step is repeated once with a penetration time of 1 min to infiltrate remaining porosities.
To avoid behavioral changes of participants with regard to oral hygiene, we will not inform them about the treatment allocation of their teeth. To ensure blinding, we perform a placebo treatment on control teeth: Instead of HCl-gel and infiltrant, water is used. Fluoridation, oral hygiene, and dietary instructions are given to the patients.
After the application of the infiltrant,and restoration,we will check with DIAGNOcam and Bitewing radiography again,because we have no idea about the characteristics of the DIAGNOcam image after resin infiltration.
2.6 Follow-up Examination Every three months since then, participants will be re-called for follow-up examination. DIAGNOcam and bitewing examinations are operated by the same investigator(WF) and the same experienced dental assistant .
Clinical examination and caries risk assessment are performed by one clinical investigator (YCC), who is blinded with regard to treatment group allocation of teeth.
The primary outcome is the progression of lesion depth, assessed by pair-wise comparison DIAGNOcam and pair-wise comparison of the bitewing radiographs .
Secondary outcome
- Patients will be interviewed for possible unwanted side-effects.
- Participant and operator perception, as measured by standardised/validated questionnaires
- The sensitivity of DIAGNOcam and bitewing radiography in monitoring caries' progression.
Additional follow-up examinations are planned 24 and 36 months after intervention.
If a lesion of any group progresses during the follow-up period radiographically to the D2 or D3 stage, restorative treatment will be performed.
In order to allow for reproducible DIAGNOcam geometry, the handled camera keeps vertical to the tooth long axis.
DIAGNOcam images as well as bitewing radiographs will be assessed by two reviewers(SC,XYJ) independently (inter-examiner reliability was assessed), both of whom are blinded with regard to treatment group allocation. Both assessors attend a training and calibration session one day prior to examination. By anonymising the radiographs, masking the stage of treatment (i.e. baseline or follow-up) or both to ensure adequate blinding of assessors.First, the DIAGNOcam and radiographic stage (E1-D3) of lesions at baseline and follow-up examination was assessed. Subsequently, examiners read the DIAGNOcam images and radiographs pairwise and judged whether lesions showed progression, regression, or were stable. In cases of different interpretation between examiners, a consensus rank was agreed. To assess intra-observer reliability, we repeated the readings after 4 wks.
3.Statistical Analysis Inter- as well as intra-observer reliability was assessed by kappa statistics. We used the X2test to analyze differences between treatment and control groups with regard to lesion progression (pair-wise comparison using DIAGNOcam and bitewing).
- Conditions
- Caries; Initial
- Being tested
- resin infiltration, remineralization, sham
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
resin infiltrationOther
using infiltrant resin intervene proximal caries
remineralizationOther
using fluoride to remineralize proximal caries
shamOther
replace resin with water
| Study group | Role | What they receive |
|---|---|---|
| resin infiltration | Experimental | resin infiltrant (Icon product, DMG, Hamburg,Germany) Receives: Other: resin infiltration |
| remineralization | Active comparator | Not described Receives: Other: remineralization; Other: sham |
What is being measured
The primary outcome is the main question the study is designed to answer.
pairwise bitewing radiograph and DIAGNOcam image
comparing the outcome of bitewing radiograph and DIAGNOcam image of pre- and post- operation
Measured: after three years
Secondary outcomes (1)
compare the cost-effectiveness between resin infiltration and remineralization
calculate the consumption of infiltrant and Duraphat,combined with the effectiveness
Measured: after three year years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Sep 2019
- Study start10 Aug 2018
- Primary completion10 Dec 2019 (estimated)
- Study completion10 Aug 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Caries; InitialStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 37 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Wuhan University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Fei Wang, Wuhan University
- Investigators
- liuyan meng, dovtor, Principal investigator, Hospital of Stomatology, Wuhan University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04092296
- Sponsor's protocol ID
- 20180103
- Acronym
- RIDCBW
- Status last verified
- Sep 2019
- First submitted
- 14 Sep 2019
- Last updated
- 17 Sep 2019
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Sep 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy of Resin Infiltration of Proximal Caries Tested With DIAGNOcam and Bitewing Radiography:Randomized Controlled Clinical Trial
- ClinicalTrials.gov ID
- NCT04092296
- Acronym / sponsor ID
- RIDCBW / 20180103
- Conditions
- Caries; Initial
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 37 participants (estimated)
- Lead sponsor
- Wuhan UniversityUniversity, hospital or other
- Study start
- 10 Aug 2018 (actual)
- Primary completion
- 10 Dec 2019 (estimated)
- Study completion
- 10 Aug 2021 (estimated)
- First posted
- 17 Sep 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of the present study was to assess the clinical efficacy of resin infiltration of interproximal caries lesions using a novel measure method-----DIAGNOcam. This study is conducted on adults (15-40y)with the aim of comparing the therapeutic effects of infiltrating caries lesions and fluoride remineralization treatment after 1, 2, and 3 yrs. The outcome (lesion progression) is evaluated by DIAGNOcam and radiographic techniques.And we would compare the sensitivity of monitoring progression of caries between DIAGNOcam and bitewing radiography.
Detailed description
On the baseline,At a screening visit, eligibility of interested participants is checked with DIAGNOcam by a researcher(WF),in addition,a pair of standardized conventional bitewing radiographs is taken using a film holder Kwik-Bite by a very experienced dental assistant .
two reviewers(SC、XYJ) who are trained the scoring systems score the DIAGNOcam and bitewing image independently,disagreements are solved by consensus and a final DIAGNOcam and bitewing score are given.Participants who have two E2 lesions are picked to join the first set up.
A.DIAGNOcam image scoring system:
E1:Dark shadow confined to the out half of the enamel E2:Dark shadow confined to the inner half of the enamel D1:Dark shadow reach dentin ,dentin caries penetrating the enamel-dentin junction linerly D2:Deep dentin are involved
B .bitewing radiograph scoring system:
E1 = radiolucency in the out half of the enamel; E2 = radiolucency extending to the enamel dentine junction; D1= radiolucency into dentine but limited to the outer third; D2 = radiolucency into middle or middle third of the dentine; D3 = radiolucency into middle or inner third of the dentine; 2.3 Caries risk and periodontal condition assessment On the baseline ,we use the dmft/s to asess the caries risk.In addition,Occurrence of plaque is scored as 0 = no visible plaque or 1 = visible plaque; the status of the gingiva is scored as 0 = sound, 1 = redness, with no bleeding after probing, 2 = bleeding after probing, and 3 = heavily inflamed.
2.4 Allocation From each pair, 1 lesion is allocated to the "test" and 1 to the "control" group using random number table and sealed in opaque envelope to prevent the allocation being known in advance of, or during, enrolment 2.5 Treatment INTERVENTION 1:Resin infiltration:Treatment is performed by a single trained investigator (WF) at the Wuhan University stomatological Hospital . A rubber dam is applied to achieve dry working conditions. In the test group, allocated teeth are slightly separated by plastic wedges (Wedge Wands, small or medium; Garrison, Übach-Palenberg, Germany) that have been flattened by a scalpel to leave space below the contact point. A piece of polyurethane foil is placed in the contact area with a plastic holder to protect the adjacent tooth. A 15% HCl etching gel (Icon product, DMG, Hamburg,Germany) is applied by syringe in the area below the contact point for 120 sec. Subsequently, the gel is washed off with air-water-spray for 30 sec. The lesion is desiccated by air-blowing for 30 sec, application of ethanol for 30 sec, and air- blow ing again for 30 sec. An infiltrant (Icon product,DMG) is applied with another plastic holder,in this time the investigator need to shut off the light.. After 3 min of penetration time, excess material is removed by air blowing and flossing, and the resin is light-cured for 1 min from the buccal, occlusal, and oral aspects. The infiltration step is repeated once with a penetration time of 1 min to infiltrate remaining porosities.
To avoid behavioral changes of participants with regard to oral hygiene, we will not inform them about the treatment allocation of their teeth. To ensure blinding, we perform a placebo treatment on control teeth: Instead of HCl-gel and infiltrant, water is used. Fluoridation, oral hygiene, and dietary instructions are given to the patients.
After the application of the infiltrant,and restoration,we will check with DIAGNOcam and Bitewing radiography again,because we have no idea about the characteristics of the DIAGNOcam image after resin infiltration.
2.6 Follow-up Examination Every three months since then, participants will be re-called for follow-up examination. DIAGNOcam and bitewing examinations are operated by the same investigator(WF) and the same experienced dental assistant .
Clinical examination and caries risk assessment are performed by one clinical investigator (YCC), who is blinded with regard to treatment group allocation of teeth.
The primary outcome is the progression of lesion depth, assessed by pair-wise comparison DIAGNOcam and pair-wise comparison of the bitewing radiographs .
Secondary outcome
- Patients will be interviewed for possible unwanted side-effects.
- Participant and operator perception, as measured by standardised/validated questionnaires
- The sensitivity of DIAGNOcam and bitewing radiography in monitoring caries' progression.
Additional follow-up examinations are planned 24 and 36 months after intervention.
If a lesion of any group progresses during the follow-up period radiographically to the D2 or D3 stage, restorative treatment will be performed.
In order to allow for reproducible DIAGNOcam geometry, the handled camera keeps vertical to the tooth long axis.
DIAGNOcam images as well as bitewing radiographs will be assessed by two reviewers(SC,XYJ) independently (inter-examiner reliability was assessed), both of whom are blinded with regard to treatment group allocation. Both assessors attend a training and calibration session one day prior to examination. By anonymising the radiographs, masking the stage of treatment (i.e. baseline or follow-up) or both to ensure adequate blinding of assessors.First, the DIAGNOcam and radiographic stage (E1-D3) of lesions at baseline and follow-up examination was assessed. Subsequently, examiners read the DIAGNOcam images and radiographs pairwise and judged whether lesions showed progression, regression, or were stable. In cases of different interpretation between examiners, a consensus rank was agreed. To assess intra-observer reliability, we repeated the readings after 4 wks.
3.Statistical Analysis Inter- as well as intra-observer reliability was assessed by kappa statistics. We used the X2test to analyze differences between treatment and control groups with regard to lesion progression (pair-wise comparison using DIAGNOcam and bitewing).
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| resin infiltration | Experimental | Other: resin infiltrationresin infiltrant (Icon product, DMG, Hamburg,Germany) |
| remineralization | Active comparator | Other: remineralization, Other: sham |
Who may qualify
- Ages
- 15 to 40 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (1 listed)
- individuals who want to participate in the study ,the presence of 2 or more non-cavitated interproximal caries lesions with dark shadow involved in the enamel on the DIAGNOcam image -
Key exclusion criteria (1 listed)
- patient who diagnosed with dentinogenesis imperfecta
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| resin infiltrationusing infiltrant resin intervene proximal caries | Other | resin infiltration |
| remineralizationusing fluoride to remineralize proximal caries | Other | remineralization |
| shamreplace resin with water | Other | remineralization |
Primary outcome
pairwise bitewing radiograph and DIAGNOcam image
Time frame: after three years
comparing the outcome of bitewing radiograph and DIAGNOcam image of pre- and post- operation
1 secondary outcome
compare the cost-effectiveness between resin infiltration and remineralization
Time frame: after three year years
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Sep 2019.
Related trials for Caries; Initial
Active, not recruiting
A Split-Mouth Clinical Trial Evaluating the Bond Failure Rate of a New Etch-Free Orthodontic Adhesive
Bracket Bonding, Orthodontic Treatment
Not yet recruitingObservational study
Artificial Intelligence Versus Clinical Examination in White Spot Lesions Detection, Identification, And Scoring
White Spot Lesion of Tooth
Recruiting
EFFICACY OF BIOMIN FLUORIDE VERSUS SODIUM FLUORIDE VARNISHES, WITH AND WITHOUT DIODE LASER ON WHITE SPOT LESIONS REMINERALIZATION IN PRIMARY TEETH.
White Spot Lesions [Initial Caries] on Smooth Surface of Tooth
Not yet recruiting
S-PRG Filler for Preventing White Spot Lesions During Orthodontic Treatment
White Spot Lesion of Tooth, Orthodontic Treatment
Active, not recruiting
The Effect of an Adhesive System on the Retention and Caries Prevention for Fissure Sealants in Permanent Molars
Dental Caries, Fissure Sealant
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
liuyan meng, dovtor principal investigator
Hospital of Stomatology, Wuhan University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing resin infiltration and remineralization in people with Caries; Initial, run by Wuhan University at 1 site in China.
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 1 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 17 Sep 2019. 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 China. 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 fei wang (15927529467, 121565382@qq.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
pairwise bitewing radiograph and DIAGNOcam image (time frame: after three years). 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 17 Sep 2019.