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comparison of oro-antral fistula closure techniques

The comparison of success of using "titanium mesh with buccal advancement flap" for oro-antral fistula closure in compare with "buccal fat pad and buccal advancement flap"

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200922048799N1
Enrollment
12
Registered
2021-10-03
Start date
2021-09-23
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

oro-antral fistula. Unspecified lesions of oral mucosa

Interventions

Intervention 1: Intervention group: titanium mesh and buccal advancement flap. Intervention 2: Control group: buccal fat and buccal advancement.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with OAF over 18 years, symptoms of maxillary sinusitis, ASA 1 and 2, OAF larger than 5 mm OLD (one month to 6 months after fistula)

Exclusion criteria

Exclusion criteria: Patients under 18 years, ASA above 2, previous failed treatments, history of microvascular and post-diabetes microvascular, metabolic bone disorders, history of renal failure, head and neck radiotherapy, patients under chemotherapy, pregnancy, drug or alcohol use, poor oral hygiene, periodontal disease, a gingival bleeding index above 20% maxillary fracture, presence of fixation devices or foreign bodies in the sinus, medication-related osteonecrosis of the jaw (MRONJ), or the presence of osteoradionecrosis. patients who refuse to participate in follow-up sessions

Design outcomes

Primary

MeasureTime frame
Wound dehiscence in clinical observation,. Timepoint: one-week, one-month, three-month, and six-month. Method of measurement: clinical observation.;Infection in clinical observation,. Timepoint: one-week, one-month, three-month, and six-month. Method of measurement: infection signs including edema, erythema, pus or hotness.;Swelling in clinical observation,. Timepoint: one-week, one-month, three-month, and six-month. Method of measurement: clinical evaluation.;Oro-antral fistula in clinical observation,. Timepoint: one-week, one-month, three-month, and six-month. Method of measurement: clinical evaluation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPouria Javaheri

Shahid Beheshti University of Medical Sciences

pouriajavaheri1371@gmail.com+98 21 4044 3580

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026