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Use of soft-tissue substitutes in the treatment of exposed rooth tooth

Use of xenogenic soft-tissue substitutes in the treatment of gingival recessions: A controlled randomized trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-106mfmx6
Enrollment
Unknown
Registered
2021-12-02
Start date
2022-01-02
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Tooth abrasion

Interventions

Experimental Group 1: 16 patients with Miller class I or II gingival recession associated with tooth abrasion who will be treated with Porcine Collagen Matrix Experimental Group 2: 16 patients with Mi

Sponsors

Universidade Federal de Uberlândia
Lead Sponsor
Universidade Federal de Uberlândia
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Present a single or multiple gingival recessions classified as RT1 (Miller class I and II) that require surgical treatment; Lack of previous experience with surgical treatment to treat gingival recessions; Ability to maintain good oral hygiene; Presence of non-carious cervical lesions associated with at least one of the gingival recessions; Being systemically healthy or having compensated systemic diseases; Present age between 18-60 years old.

Exclusion criteria

Exclusion criteria: History of untreated periodontal disease; Cigarette consumption greater than 10 units per day; Furcation lesion on the tooth to be treated; Presence of severe crowding, rotation or poor positioning of the tooth to be treated; Hypersensitivity to any anesthetic, medication or antiseptic product used in surgery; Medical limitation for elective surgical procedures; Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Evaluate the vertical coverage of the exposed root surface and percentage of root coverage, considering that one treatment will be superior to the other if there is more than 1 mm of root coverage or more than 20% of root coverage percentage.

Secondary

MeasureTime frame
Evaluate the probing depth and the clinical attachment level considering that one treatment will be superior to the other if the probing depth is reduced by 1 mm and the clinical insertion level increased by 1 mm.;Evaluate the thickness of the keratinized mucosa and the height of the keratinized mucosa, considering that one treatment will be superior to the other if there is an increase in the thickness of the mucosa by 0.5mm and an increase in the height of the mucosa of the keratinized mucosa by 1 mm.;Evaluate aesthetics through a score in which one treatment will be superior to the other if there are differences of at least 3 points in that score.;Evaluate the surgery time as one treatment will be superior to the other if you reduce the surgery time by 5 minutes.

Countries

Brazil

Contacts

Public ContactGuilherme Oliveira

Universidade Federal de Uberlândia

guilherme.lopesoliveira@ufu.br+55(34)32258132

Outcome results

None listed

Source: REBEC (via WHO ICTRP)