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Marsupialization of Odontogenic Cysts

Novel Use of Grommet Tube in the Treatment of Odontogenic Cysts Marsupialization

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07277959
Enrollment
10
Registered
2025-12-11
Start date
2025-01-02
Completion date
2025-10-20
Last updated
2025-12-11

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

Conditions

Odontogenic Cysts Marsupialization

Brief summary

To evaluate the efficacy of the Grommet tube by measuring the rate of reduction in cyst size, assess patients satisfaction, and evaluate the occurrence of complications.

Interventions

DEVICEnovel use of Grommet tube

The intervention consisted of performing conventional marsupialization of the odontogenic cyst followed by the novel placement of a ventilation Grommet tube to maintain long-term patency of the surgical window. After administration of local anesthesia, a small bony window was created over the thinnest cortical area of the cyst to expose the cystic cavity. The cyst lining was incised then the tube was placed

Sponsors

University Of Anbar
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Pathological diagnosis of odontogenic cyst * Indicated for marsupialization * Patients aged from 15 to 60 years

Exclusion criteria

* Soft tissue cysts. * Patients with systemic diseases affecting bone healing. * Patients non-compliance with follow up visits. * Patients with a history of neck and head radiotherapy or patients on chemotherapy. * Patients taking antiresorptive drugs or corticosteroids.

Design outcomes

Primary

MeasureTime frameDescription
Reduction in Cyst Size6 monthsCyst volume will be measured using CBCT and 3D Slicer segmentation at baseline and 6 months after marsupialization. Percentage reduction in cyst size will be calculated.
Patient SatisfactionTime Frame: 6 monthsPatient satisfaction will be assessed using a validated questionnaire (e.g., 3-point Likert scale) at 6 months.
Occurrence of ComplicationsTime Frame: 6 monthsThe presence of postoperative complications (infection, device displacement, or soft tissue overgrowth) will be recorded clinically at follow-up visits.

Countries

Iraq

Outcome results

None listed

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