LT Comparative Effectiveness of 2 Caries Treatments

ConditionDental Caries
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age62+
SponsorCase Western Reserve University

About this trial

This study is a continuation of a cluster randomized clinical trial (cRCT) conducted in 33 publicly subsidized housing facilities/sites (HUD Section 202) and other low-income housing voucher programs in NE Ohio. The Intervention Arm (18 sites) - participants received biannual silver diamine fluoride (SDF) versus the Control Arm (15 sites) where participants received atraumatic restorative treatment (ART) with glass ionomer cement (GIC) + biannual fluoride varnish (FV) application. A total of 568 participants were recruited in the original study, and 480 participants (Intervention Arm: 287, Control Arm: 193) are expected to continue in this long-term follow-up study. Since enrollment in the original study was done over time, each participant will contribute data at 3 to 6 years (from randomization) in the LTFU depending on study entry to assess clinical equipoise of the two treatments.

Community-dwelling older adults, regardless of medical, cognitive, or motor impairments, were considered for inclusion in the original study and were: (1) aged ≥ 62 years in the 33 housing facilities; (2) have at least one untreated active root or coronal carious lesion with ICDAS-II lesion severity code of 3 or greater ; (3) willingness to stay in the study for 1 year. Exclusion criteria: (1) sensitivity to silver or other heavy-metal ions; (2) serious life-threatening medical disease. Additionally, any participant with the presence of gingival/perioral ulceration or stomatitis or tooth abscess in any specific tooth were referred to a dentist and enrolled after resolution. The LTFU study will follow the same enrolled participants long-term. The current mean (sd) age of the 480 participants who will enter the LTFU study will be 73.73 (6.92) years.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Were participants in the original study from the 33 housing sites

Provide signed and dated long-term follow-up informed consent form

Willingness to stay in the LTFU study for 1 year

Additionally for focus groups, completed the treatment phase of the study

Disqualifiers

Sensitivity to silver or other heavy-metal ions

Serious life-threatening medical disease

Additionally, any participant with the presence of gingival/perioral ulceration or stomatitis or tooth abscess in any specific tooth will be referred to a dentist but can only be enrolled after resolution

Trial design

Design model

Parallel

Treatments tested in this trial

  • A "simple medical strategy" consisting of silver diamine fluoride (SDF)

    Device

    Bi-annual topical application of 38% silver diamine solution to new ICDAS lesions code 3-6. Advantage Arrest, Elevate Oral Care, West Palm Beach FL

  • A "typical dental strategy" consisting of atraumatic restorative treatment (ART) with glass ionomer cement + Fluoride Varnish (FV)

    Device

    GC Fuji (for ART) and FluoriMax Varnish. Atraumatic Restoration Treatment (ART) to new ICDAS lesions code 3-6, followed by bi-annual topical fluoride varnish (FV) to all teeth.

Treatment groups

480 Participants
are divided into 2 treatment groups
Group A: A "simple medical strategy" consisting of SDFExperimental treatment 1 intervention
Group B: A "typical dental strategy" consisting of ART + FVActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Caries Arrest Rate

ICDAS examinations are used to assess caries arrest on permanent tooth surfaces with moderate to severe lesions (ICDAS codes 3-6 with activity code 2) that received SDF or ART + FV treatment. A lesion is considered arrested if, at follow-up, the activity code is 1 (inactive) or the surface is sound (code S). The overall mean will be calculated by surfaces.

Time frame
Baseline (LTFU 1) to 52-weeks (LTFU 3)
2

New Decay Rate

New decay is defined as ICDAS lesion code ≥3 (localized to extensive decay) on one or more surfaces on newly decayed teeth found at LFTU #1, #2 and #3 (even on surfaces that did not receive the study treatments). The overall mean of decayed surfaces will be calculated.

Time frame
Baseline (LTFU 1) to 52-weeks (LTFU 3)
3

Tooth Loss

Tooth loss will be assessed through ICDAS exams by documenting absence of teeth. The overall mean will be calculated for the number of teeth lost.

Time frame
Baseline (LTFU 1) to 52-weeks (LTFU 3)
4

Tooth Pain

Tooth Pain and Sensitivity will be assessed using the PROMIS v.1.0 - Pain Intensity 3a \[Modified for Dental\]. An overall mean pain intensity score will be created for the 3-item Likert scale with answers ranging from 0-no pain to 4-very severe.

Time frame
Baseline (LTFU 1) to 52-weeks (LTFU 3)

Secondary outcomes

1

Gingival Inflammation Index

Gingival inflammation will be assessed using the Modified Gingival Index. Scores range from 0-4, with 0 being healthy gums, 1-mild inflammation, 2-moderate inflammation, and 3 and 4 (more bleeding and ulceration) being severe inflammation. The mean overall scores will be calculated.

Time frame
Baseline (LTFU 1) to 52-weeks (LTFU 3)

Other outcomes

Sponsors and contacts

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Case Western Reserve University

Lead sponsor

Patient-Centered Outcomes Research Institute

Collaborator