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resorption of cancellous versus corticocancellous bone graft in unilateral alveolar cleft defect.

Not Applicable
Completed
Conditions
Health Condition 1: Q188- Other specified congenital malformations of face and neck
Registration Number
CTRI/2020/09/028001
Lead Sponsor
Dr Bhavana valvi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

Patients should be non syndromic

Patients with unilateral cleft of alvelous previously operated for primary cleft lip and palate defect

Patients medically fit to undergo general anesthesia

Exclusion Criteria

Patients with bilateral cleft alveolus

Patients with systemic disease contraindicating general and local ansthesia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To check the upatake of either cancellous or corticocancellous bone graft <br/ ><br>is more or equal in secondary alveolar cleft defect <br/ ><br>To observe the site and architecture of the newly formed bone after grafting <br/ ><br>To see the actual amount of bone uptake <br/ ><br>To see the alar base support for the ala after graftingTimepoint: 6 months of follow up in 18 months of duration
Secondary Outcome Measures
NameTimeMethod
To check the efficiency of cancellous and corticocancellous bone graft <br/ ><br>To observe the site and architecture of newly formed bone after grafting <br/ ><br>To check actual amount of bone uptake <br/ ><br>To see the alar base support for the ala after graftingTimepoint: 6 months of follow up in 18 months of duration
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