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Surgical Extrusion for the Clinical Crown Lengthening: a 12-months Clinical Study

Surgical Extrusion for the Clinical Crown Lengthening: a 12-months Prospective Clinical Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04350853
Enrollment
11
Registered
2020-04-17
Start date
2018-03-20
Completion date
2020-03-15
Last updated
2020-04-17

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

Conditions

Tooth Decay

Keywords

extrusion

Brief summary

This is a prospective study in which surgical extrusion of single-rooted teeth is carried out by the same operator in 15 consecutive patients. Main objective: to evaluate the soft tissue rebound of the teeth 1 year after the surgery. Null hypothesis (H0): surgical extrusion is not a predictable treatment for the restoration of single rooted teeth.

Interventions

Surgically coronal reposition of the tooth

Sponsors

Universitat Internacional de Catalunya
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Systemically and periodontally healthy, non-smoking patients. * Single-rooted, straight teeth with insufficient ferrule, which require restorative treatment. * Teeth with a favorable crown-root ratio.

Exclusion criteria

* Severe systemic disease patients (American Society of Anesthesiologists classification 1 or 2). * Multi-rooted, curved and/or short teeth. * Teeth with an uncontrolled periodontal pathology. * Pregnant women. * Teeth with types ll or lll mobility.

Design outcomes

Primary

MeasureTime frameDescription
Soft tissue rebound12 months after the surgical extrusionmm
Tooth mobility (Miller classification)12 months after the surgical extrusionmm
Periapical lesion occurrence12 months after the surgical extrusionAssessed as the presence or not of a radiolucency at periapical radiograph (yes/no)
Patient's response to pain or discomfort at percussion test12 months after the surgical extrusionPatient's response measured by yes/no
Patient's response to pain or discomfort at palpation test12 months after the surgical extrusionPatient's response measured by yes/no
Root resorption occurrence12 months after the surgical extrusionAssessed as the presence or not of an inflammatory root resorption and a replacement root resorption at periapical radiograph

Secondary

MeasureTime frameDescription
Periodontal probing12 months after the surgical extrusionmm
Patient's satisfaction12 months after the surgical extrusionMeasured visually using a visual analogue scale, in which the best score is 0 (highest level of patient's satisfaction) and the worst score is 10 (lowest level of patient's satisfaction).
Gum bleeding on periodontal probing (yes/no)12 months after the surgical extrusionVisual
Tooth plaque quantity12 months after the surgical extrusionMeasured visually according to Turesky plaque index, in which the best score is 0 (no plaque) and the worst score is 5 (plaque covering 2/3 or more the crown of the tooth).
Interproximal papillae height12 months after the surgical extrusionMeasured visually according to Jemt's index, in which the best score is 3 (interproximal space completely occupied) and the worst score is 0 (absent interproximal papilla).
Marginal bone loss12 months after the surgical extrusionmm
Crown-root ratio12 months after the surgical extrusionmm

Countries

Spain

Outcome results

None listed

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