Last reviewed · How we verify
NCT04922086
Digital Planning and Guided Dual Technique in Aesthetic Crown Lengthening
NA trial testing Conventional aesthetic crown lengthening surgery in Tooth Eruption Disorder in 24 participants. Completed in 1 August 2021.
1 July 2021
Quick facts
| Lead sponsor | Universidade Federal de Alfenas |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 24 |
| Start date | 19 September 2019 |
| Primary completion | 1 July 2021 |
| Estimated completion | 1 August 2021 |
| Sites | 1 location across Brazil |
Drugs / interventions tested
- Conventional aesthetic crown lengthening surgery
- Guided dual aesthetic crown lengthening surgery
Conditions studied
- Tooth Eruption Disorder — all drugs for Tooth Eruption Disorder →
Sponsor
Universidade Federal de Alfenas — full company profile →
Who can join
Adults 18 to 50, any sex, with Tooth Eruption Disorder. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Excessive gingival exposure, commonly named gingival smile, results in a dentogingival disharmony. One of the gingival smile treatment is the aesthetics-related crown lengthening surgery (ACL) to provide a adequate clinical crown length and diminish gingival display. In this context, digital planning and guided dual technique have been proposed to increase the effectiveness and predictability of the ACL. In this technique, an facial and dental analysis of the patient is performed and transferred to a digital model obtained by intraoral digital scan. The digital model is used to create a double guide that will determine the final position of the gingival and alveolar margin in the ACL. Despite the technique showing promising results, clinical studies evaluating the effectiveness of this technique are scarce. The present study aims to evaluate the digital planning and guided dual technique in the ACL in comparison to conventional technique in relation to the predictability/stability of the gingival margin positioning and patient satisfaction after the ACL. Twenty-four patients diagnosed with altered passive eruption type I subcategory B will be selected and divided into two groups. In the control group (n = 12) patients will be submitted to the conventional ACL planned using clinical examination; in the test group (n = 12) patients will be submitted to ACL using cone beam computed tomography (CBCT), digital planning and guided dual technique. Periodontal clinical parameters including probing depth (PS), clinical attachment level (CAL), clinical crown length (CCL), anatomical crown length (ACL) and cemento-enamel junction to alveolar bone crest distance will be evaluated clinically at baseline, in the immediate postoperative, 4, 8 and 12 months after the procedure. Participants will be submitted to questionnaires to assess satisfaction with the smile, gum and tooth characteristics and experience with the procedure. The investigators aim to demonstrate with the study the effectiveness of the both techniques and evaluate the clinical cost benefit for the patient and the dentist of the guided dual technique in relation to the conventional ACL technique.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Digital planning and guided dual technique in esthetic crown lengthening: a randomized controlled clinical trial.
Carrera TMI, Freire AEN, de Oliveira GJPL, Dos Reis Nicolau S, et al · · 2023 · cited 15× · PMID 36409356 · DOI 10.1007/s00784-022-04780-8
Verify or expand the search:
- PubMed search for NCT04922086
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Universidade Federal de Alfenas trials
Trials by the same sponsor.
- NCT05989217 — Conservative Therapies in the Treatment of Temporomandibular Disorders · NA · active not recruiting
- NCT06731777 — Oral Gel Containing PHTALOX® as an Adjuvant in the Treatment of Periodontal Disease · NA · active not recruiting
- NCT05363241 — Management of Knee Pain by Cooled Radiofrequency in Classical Anatomical Targets and Revised Targets · NA · completed
- NCT05119283 — Clinical Study of a Formulation Containing Phtalox® in Periodontal Disease · NA · completed
- NCT05270161 — The Tunnel Technique and Free Gingival Graft in Gingival Recessions Treatment · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04922086 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Universidade Federal de Alfenas
- Last refreshed: 10 May 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04922086.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing