CompletedNot Applicable

Bone Lid Technique Versus Standard Technique for Treatment of Mandibular Lesions

Egypt24 participantsStarted 2023-06-20

Plain-language summary

Twenty patients with benign mandibular lesion will be included in this study. the patient will be divided randomly (10 patients each group). Group I the lesion will be treated using bone lid technique. Group II the lesion will be treated using the standard technique. The patients will be received, clinically and radiologically examined, and managed at the Oral and Maxillofacial surgery Department, Faculty of Dentistry, Tanta University. The patients will be evaluated clinically to evaluate healing and radiographically using cone beam CT (CBCT) scan to identify bone healing, the extension and the volume of lesion six months later

Who can participate

Age range

6 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: age ≥ 6 years * presence of bony lesion (cysts, benign tumors, odontoma) located in mandibular region, * the existence of a normal residual buccal cortical plate with the adequate thickness (≥1 mm) at least at the periphery of buccal cortical plate Exclusion Criteria: * • patients taking medications that affect bone metabolism, * patients underwent head and neck radiotherapy

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

degree of pain evaluated clinically in both groups

Timeframe: one-two weeks

soft tissue healing evaluated clinically in both groups

Timeframe: one week

infection evaluated clinically in both groups

Timeframe: one week-one month

cyst area calculation radiographically in both groups

Timeframe: six months

measuring the distance between the lesion and alveolar crest in both groups

Timeframe: six months

density of bone calculated radiographically in both groups

Timeframe: six months

Trial details

NCT IDNCT05987930

SponsorTanta University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-10-30

View on ClinicalTrials.gov More Mandible Cyst trials

Plain-language summary

Who can participate

Age range

6 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

degree of pain evaluated clinically in both groups

Timeframe: one-two weeks

soft tissue healing evaluated clinically in both groups

Timeframe: one week

infection evaluated clinically in both groups

Timeframe: one week-one month

cyst area calculation radiographically in both groups

Timeframe: six months

measuring the distance between the lesion and alveolar crest in both groups

Timeframe: six months

density of bone calculated radiographically in both groups

Timeframe: six months