Actively Recruiting
Treatment of Mandibular Bone Cyst by Navigation and Endoscopy
Led by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University · Updated on 2024-08-22
122
Participants Needed
1
Research Sites
123 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In this study, with the assistance of endoscopic technology and intraoperative navigation technology, the removal and curettage of large odontogenic jaw cyst occurred in the mandible were performed to reduce the rate of postoperative nerve injury. In this study, the investigators compared the efficacy of traditional extraction and curettage with endoscopic navigation assistance in the treatment of giant mandibular bone cysts. In this study, the rate of inferior alveolar nerve injury 1 month after surgery was taken as the main outcome index, and the recurrence rate 1 year after surgery was taken as the secondary outcome index, to explore whether endoscopic combined with intraoperative navigation-assisted treatment of giant mandibular bone cyst could achieve lower postoperative nerve injury rate and postoperative recurrence rate.
CONDITIONS
Official Title
Treatment of Mandibular Bone Cyst by Navigation and Endoscopy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 75 years
- Imaging and biopsy confirmed odontogenic cyst in the mandible
- Cyst is 2 cm or larger and involves the inferior alveolar nerve
- New or recurrent cysts, or cysts larger than 2 cm after previous treatment affecting the nerve
- No serious systemic diseases and can tolerate general anesthesia
- Scheduled for surgical treatment of mandibular bone cyst under general anesthesia
- No inferior alveolar nerve injury before surgery
- No participation in other clinical trials within 30 days
- Willing to volunteer and sign informed consent
You will not qualify if you...
- Severe systemic disease or pregnancy preventing tolerance to surgery and anesthesia
- Unable to complete the study due to personal, social, or economic reasons
- Psychiatric disorders or inability to communicate or cooperate, such as schizophrenia or claustrophobia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
WangYan
Guangzhou, Guangdong, China, 510000
Actively Recruiting
Research Team
Y
Yan Wang
CONTACT
Y
YILIN HE
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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