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Active, not recruitingNCT07929454ClinicalTrials.gov record

Evaluation of Orthodontic Bands Coated With Nano-silver Fluoride

White Spot Lesion of Tooth · Pocket, Periodontal · Dental Caries Tooth Demineralization

THE QUICK READ

What this study involves

The registry does not currently label this study as recruiting. Ask about its status before planning a screening visit.

Study type
Interventional
Phase
Not applicable
Age range
Not specified - Not specified
Sex eligible
All sexes
Healthy volunteers
Accepted
Participants
25 Actual

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

1. Aim of the Study To evaluate the antibacterial and enamel remineralization effects of nano-silver fluoride-coated orthodontic bands compared with conventional non-coated bands in orthodontic patients over 6 months.
2. What Will I Do in This Study?

* Conduct a randomized split-mouth clinical trial involving 25 patients.
* Place orthodontic bands on the maxillary first molars, with one band coated and the contralateral band left uncoated as the control.
* Randomize the right or left side receiving the coated band.
* Collect dental plaque samples after 24 hours, 3 months, and 6 months to measure bacterial counts, particularly Streptococcus mutans, using colony-forming unit (CFU) counting.
* Assess enamel demineralization and remineralization using DIAGNOdent measurements before band placement and after band removal.
3. Materials Used

  • Orthodontic bands: Stainless steel molar bands.
  • Silver nanoparticles (AgNPs): Concentration of 5 µg/mL, with an average particle size of 40 nm.
  • Fluoride: Concentration of 5 ppm.
  • Coating technique: Dip coating, followed by air-drying and incubator drying.
Read the full description

1. Background Fixed orthodontic appliances, particularly orthodontic molar bands, contribute significantly to increased plaque retention and bacterial accumulation around the teeth. This heightens the risk of enamel demineralization and the formation of white spot lesions (WSLs). Streptococcus mutans is considered one of the primary etiologic agents in this process, owing to its ability to produce acids that lower plaque pH and initiate enamel demineralization.

Because conventional preventive measures rely heavily on patient compliance and optimal oral hygiene, research has shifted toward developing orthodontic materials with intrinsic antibacterial properties. Nano-Silver Fluoride (NSF)-which combines silver nanoparticles with fluoride-presents a promising agent, as it is expected to reduce bacterial colonization while promoting enamel remineralization. However, clinical evidence evaluating its direct application as a coating on orthodontic molar bands remains limited.
2. Aim of the Study This split-mouth clinical trial aims to evaluate the antibacterial efficacy and enamel remineralization potential of stainless steel orthodontic molar bands coated with Nano-Silver Fluoride compared to uncoated bands during active orthodontic treatment.
3. Interventions This study will be conducted on 25 patients using a split-mouth design, where each patient will receive a coated molar band on one maxillary first molar and an uncoated band on the contralateral maxillary first molar, with side allocation determined through randomization.

Experimental Group: Stainless steel molar bands coated with a Nano-Silver Fluoride solution containing silver nanoparticles (5 µg/mL concentration, 40 nm particle size) and fluoride (5 ppm concentration).

Control Group: Conventional, uncoated stainless steel molar bands.

Coating Method: Dip-coating technique, where the bands are thoroughly cleaned, submerged in the NSF solution for a specified duration, air-dried, and subsequently oven-dried to ensure a stable coating layer.

Assessment of Antibacterial Effect: Plaque samples will be collected from the area surrounding the bands to quantify Streptococcus mutans levels using Colony-Forming Units (CFU) at 24 hours, 3 months, and 6 months.

Assessment of Enamel Remineralization: Changes in white spot lesions and enamel demineralization levels will be measured using DIAGNOdent before band placement and after band removal according to the study's follow-up schedule.
4. Summary / Conclusion This study investigates the feasibility of transforming orthodontic molar bands from passive mechanical retention devices into active preventive components that combine antibacterial activity with the preservation of enamel integrity during orthodontic therapy.

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

Inclusion Criteria:

  • • Patients presenting with malocclusion, including crowding, spacing, increased overjet or overbite, crossbite, or open bite.
  • Presence of a sufficient number of erupted permanent teeth to allow effective placement and retention of orthodontic appliances.
  • Good oral and periodontal health, with no active caries or untreated periodontal disease.
  • Systemically healthy patients, or those with controlled medical conditions that do not contraindicate orthodontic tooth movement.
  • Patients demonstrating adequate motivation and willingness to cooperate, including maintaining oral hygiene and attending regular follow-up visits.

Exclusion Criteria:

  • • Presence of active dental caries or Poor oral hygiene.
  • Active periodontal disease, including gingivitis or periodontitis with attachment loss.
  • Patients with uncontrolled systemic diseases that may affect bone metabolism or healing (e.g., uncontrolled diabetes, metabolic bone disorders).
  • Use of medications that adversely affect orthodontic tooth movement and cannot be medically managed.
  • Insufficient erupted teeth to support orthodontic appliances.
  • Low motivation or poor compliance, including failure to attend appointments or follow treatment instructions.
Understand screening

Treatment, groups and participation

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Assignment
Random assignment
Masking
Double masked
Nano-silver Fluoride Coated Orthodontic Bands

Participants receiving orthodontic bands coated with Nano-silver Fluoride (NSF).

Device: Nano-silver Fluoride Coated Orthodontic Bands

Uncoated Orthodontic Bands

Participants receiving conventional uncoated orthodontic bands.

Other: Conventional Uncoated Orthodontic Bands

Nano-silver Fluoride Coated Orthodontic Bands DEVICE

Orthodontic bands coated with Nano-silver Fluoride (NSF) solution applied to cementation to evaluate antibacterial and remineralization effects.

Conventional Uncoated Orthodontic Bands OTHER

Standard uncoated orthodontic bands were used as a control group.

Prepare your questions

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Change from baseline in Streptococcus mutans count in plaque around the band

Time frame: Baseline, 3 months, and 6 months post-placement.

Plaque samples will be collected from around the orthodontic band to quantify Streptococcus mutans levels using Colony Forming Units (CFU/mL) count.

Secondary measures

Remineralization Effect

Time frame: Baseline, 3 months, and 6 months post-placement.

The incidence and severity of white spot lesions on the first molars will be assessed using laser fluorescence (DIAGNOdent).

No results are flagged as posted.

Review the complete result tables and limitations in the official record.

Open official results ↗

Research locations (1)

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1 locations

Mansoura universityAl Mansurah, EgyptStatus unknown

Study team and timeline

Lead sponsor
Ebrahim N Abbas
Study start
Aug 8, 2026 Actual
Primary completion
Feb 8, 2027 Estimated
Study completion
Mar 8, 2027 Estimated
First posted
Nov 10, 2026 Actual
Last updated
Nov 10, 2026 Actual

Official study contacts

No central contact is listed. Check the locations and the official record.

Official study title

Evaluation of Antibacterial and Remineralization Effect of Orthodontic Bands Coated With Nano-silver Fluoride: A Randomized Controlled Clinical Trial

A HUMAN NEXT STEP

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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.

Retrieved: Nov 11, 2026 · Last registry update: Nov 10, 2026