search

Active clinical trials for "Odontogenic Cysts"

Results 1-4 of 4

Decompression of Odontogenic Cysts Using an Appliance Fabricated With a Fully Digital Workflow

Odontogenic Cysts

The aim of this prospective case series is to present clinical results with cystostomy, decompression and final enucleation of odontogenic cysts using a decompression device fabricated with a full digital workflow and delivered on the day of cystostomy. The secondary purpose of our study is to present the volumetric changes of the odontogenic cysts treated by decompression.

Recruiting4 enrollment criteria

The Evaluation of the Effect of Performing Guided Lid Surgery

Odontogenic Cysts

to evaluate the percentage of bone volume regain along with postoperative pain in cases done using the bone lid technique in comparison with those done using the conventional cyst enucleation technique.

Recruiting6 enrollment criteria

Recurrence of Odontogenic Keratocyst

Odontogenic Cyst

The aim of current cross over clinical trial is to evaluate the effect of topical 5-FU as adjunct therapy in reducing risk of the recurrence of OKCs

Enrolling by invitation2 enrollment criteria

Usage of 5-fluorouracil and Carnoy's Solution in Surgical Treatment of Odontogenic Keratocysts

Odontogenic Keratocyst

The goal of this clinical trial is to compare surgical treatment outcomes of odontogenic keratocysts (OKC) treated with enucleation and local application of Carnoy's solution or 5% 5-fluorouracil. The main questions it aims to answer are: What is the recurrence rate of OKC treated with enucleation and local application of 5% 5-fluorouracil cream in the period of three and five years after the treatment What is the recurrence rate of OKC treated with enucleation and local application of Carnoy's solution in the period of three and five years after the treatment Is there a difference in the recurrence rate between these two groups What is the frequency of sensitivity disorders in the innervation zone of inferior alveolar and infraorbital nerves in both groups Participants will be assigned to one of two groups after Histopathological verification (HP verification).They will be treated with enucleation and local application of Carnoy's solution or 5% 5-fluorouracil depending on group. After surgical treatment they will be monitored in accordance to standard treatment protocols for patients with OKC.

Enrolling by invitation5 enrollment criteria
1

Need Help? Contact our team!


We'll reach out to this number within 24 hrs