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A Modified Approach for the Closure of Oral Sinus Communications

A Modified Approach for the Closure of Oral Sinus Communications

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04499144
Enrollment
18
Registered
2020-08-05
Start date
2020-06-26
Completion date
2020-07-27
Last updated
2020-08-10

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

Conditions

Surgery Site Fistula

Keywords

Extraction, Oro-antral communication, Oro-antral fistula

Brief summary

The aim of this study is to describe a modified surgical approach for the closure of oral sinus communications, using a buccal trapezoidal flap combined with a connective pedicle flap rotated from the palate

Interventions

PROCEDUREmodified buccal flap and subepithelial connective palatal flap

The connective flap was harvested from the deeper area of the palatal mucosa. Pedicle flap dimensions were reported using the periodontal probe. The flap was then rotated to cover the oro antral communication (OAC) area. The rotation could be in mesial or distal direction, related to OAC position and for the convenience of the donor site. The connective palatal flap was sutured to the buccal periostium using mattress sutures.

Sponsors

University of Siena
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

case series of a new surgical design

Eligibility

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

Inclusion criteria

* Patient with diagnosis of Oro-antral communication * Patients with adequate radiographic status * Patients who read and signed the informed consent * Patients without periodontal disease * Patients≥18

Exclusion criteria

* Pregnancy or breastfeeding patients * Patients compliance and patients with mental disorders * Patients with diabetes * Patients with osteonecrosis * Patients with head and neck cancer

Design outcomes

Primary

MeasureTime frameDescription
Closure of the communicationDay 30Clinical observation

Secondary

MeasureTime frameDescription
Pain and discomfortDay 30These parameters are described using VAS technique

Countries

Italy

Outcome results

None listed

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