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clinical trial to evaluate the safety and efficacy of domestic absorbable membrane and foreign absorbable memrane targeting periontal disease patient needed guided bone regeneration.

Not Applicable
Recruiting
Conditions
Diseases of the digestive system
Registration Number
KCT0001814
Lead Sponsor
Ministry of Health & Welfare
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
58
Inclusion Criteria

? Only adults over 20 years old
? Patients need to extract teeth due to the maxillary or mandibular periodontitis

Exclusion Criteria

? periodontal disease site with acute infection.
? in case of extraction because of wide range bone loss
? pregnant woman
? Uncontrolled hypertension or with diabetes
? In patients with a history or current malignant disease jaws
? Serious cardiovascular disease, respiratory disease, heart disease, liver disease, digestive disorders, blood disorders and neurological disorders • Patients with Psychiatric Disorders and merging
? Patients with hyperthyroidism or hypothyroidism.
? Patients with a history of drug allergy
? Depression or anxiety disorder altitude, and the patient is determined to influence the efficacy
? patients with a history of drug or alcohol abuse within 1 year currently Abuse
? Patients deemed suitable by the investigator or research enforcer this study

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
evaluating the efficacy using Cone-beam CT for the measurement volume level the surrounding tissue preparatione
Secondary Outcome Measures
NameTimeMethod
Engraftment and absorption evaluation of the bone graft material using a Cone-beam CT .;evaluating the efficacy using Cone-beam CT for the measurement volume level the surrounding tissue preparatione before and after surgery.;VAS scale;Check exposure of Bone graft material and adverse Oral Evaluation
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