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Clinical Trial of Two Techniques for Gingival Displacement

A Double-blind Randomized Clinical Trial of Two Techniques for Gingival Displacement

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01848496
Enrollment
22
Registered
2013-05-07
Start date
2012-01-31
Completion date
2013-03-31
Last updated
2013-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Poor Aesthetic of Existing Restoration of Tooth

Brief summary

Regardless of the selected technique for dental impression, gingival displacement is an essential procedure specially when making impressions of subgingival finishing lines, because a moisture-free sulcus is a requirement for an effective impression. The objective of this randomized clinical study is to evaluate the efficacy of the conventional and cordless gingival displacement (GD) techniques.

Detailed description

On conventional technique we normally use a cord for gingival displacement. On the other hand, on cordless technique do not require this need.

Interventions

Gingival displacement is a dental procedure that allows exposure of the finishing line of a dental cavity in order to produce a well-adapted restoration.

Sponsors

Maximiliano Sergio Cenci
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* good general and dental health * at least two anterior teeth with an indication of prosthetic dental crown

Exclusion criteria

* smoking habits * systemic diseases * pregnant * had not consumed antibiotics or anti-inflammatory drugs in the last 60 days * the selected teeth must have good periodontal health characterized by regular gingival margin with at least 2 mm of attached gingiva, non-fibrotic gingival tissue, no marginal recession, probing depth ≤ 3 mm, no evidence of significant loss of bone insertion and present no visible plaque and gingival bleeding

Design outcomes

Primary

MeasureTime frame
Interleukins concentration on gingival crevicular fluidBefore and 1 day after gilgival displacement

Secondary

MeasureTime frameDescription
Periodontal indicesBefore, 1 day after and 10 day after gingival displacementPeriodontal indices (attachment level, gingival bleeding and plaque index) were evaluated before and after gingival displacement by the both techniques.

Other

MeasureTime frameDescription
Self-reported unpleasant flavour and painImmediatelly after interventionsAlso were evaluated subjective parameters (unpleasant flavor and pain) self-reported by the volunteers during gingival displacement. These subjective outcomes were collected using the visual analogic scale.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026