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Clinical Evaluation of Conventional Versus Microsurgical Techniques of Esthetic Crown Lengthening

Clinical Evaluation of Gingival Margin Stability Following Conventional Versus Microsurgical Techniques of Esthetic Crown Lengthening

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03804281
Enrollment
24
Registered
2019-01-15
Start date
2019-02-01
Completion date
2020-08-01
Last updated
2019-01-18

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

Conditions

Gummy Smile

Brief summary

the study compare gingival margin stability following conventional approach versus microsurgical approach of esthetic crown lengthening in management of patients with short clinical crowns in the upper anterior region.In management of patients with short clinical crowns in the upper anterior region, there is no difference in gingival margin stability between conventional and microsurgical approaches of esthetic crown lengthening.

Interventions

PROCEDURETest group

The surgery will be done with the use of 4x magnification loop, the knives are micro blades and micro-sutures 7//0 used with the microsurgical instruments kit

PROCEDUREControl group

esthetic crown lengthening with conventional approach with an internal bevel incision, following CEJ anatomy, this will be followed by an intra-sulcular incision, removal of the strip of outlined marginal gingiva and elevation of a mucoperiosteal flap to the level of the alveolar bone crest.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients with healthy systemic condition. * Adult patients ˃ 18 years old. * The presence of the six upper anterior teeth. * Absence of sites with attachment loss and probing depth (PD) \>3 mm * Keratinized gingiva of at least 2mm width. * Compliance with good oral hygiene. * Patients accepts 6-months follow-up period (cooperative patients). * Patients provides an informed consent

Exclusion criteria

* Gummy smile with normal tooth proportions * Presence of prosthetic crowns * Extensive restorations * Extensive incisal edge attrition. * Misalignment on maxillary anterior teeth. * Smokers ˃ 10 cigarettes / day.

Design outcomes

Primary

MeasureTime frameDescription
Mid-buccal gingival margin level6 monthsperiodontal probe with William's graduation will be used to measure the distance from the CEJ to the gingival margin at the mid-buccal surface

Secondary

MeasureTime frameDescription
Pink Esthetic Score (PES)6 monthsThe PES is based on seven variables: mesial papilla, distal papilla, soft-tissue level, soft tissue contour, alveolar process deficiency, soft-tissue color and texture. Each variable shall be assessed with a 2-1-0 score, with 2 being the best and 0 being the poorest score. The mesial and distal papilla will be evaluated for completeness, incompleteness or absence
Post-Surgical swelling7dayswill be evaluated post-surgically with Verbal Rating Scale with words ranging from (absent-slight-moderate-intense) Absent (no swelling), Slight (intraoral swelling at the operated area), Moderate (moderate intraoral swelling at the operated area) and Intense (intensive extra oral swelling extending beyond the operated area).
Post-Surgical Patient Satisfaction: 3-item questionnaire6 monthsA 3-item questionnaire is asked and the patients shall use a 7-point answer scale

Outcome results

None listed

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