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Evaluation of bone healing in periapical lesion by using bone repair material

Phase 4
Conditions
Health Condition 1: K099- Cyst of oral region, unspecified
Registration Number
CTRI/2022/02/040568
Lead Sponsor
Human Resource Development Group HRDG Council of Scientific and Industrial Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patient willing to participate in the study.

Periapical lesion with palatal perforation

Surgical endodontic treated reoperated (SER)

Maxillary anterior teeth

Exclusion Criteria

Periapical lesion without palatal perforation

Medically compromised OR systemic disease patient

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
This study would be able to compare the efficacy of PRF and Various bone graft material in surgical <br/ ><br>healing of periapical lesion with palatal defects <br/ ><br>It could also act as a pilot study for including PRF <br/ ><br>various Bone Graft material in main stream endo surgical healing <br/ ><br>The outcomes assessed will be <br/ ><br>Peri apical healing and <br/ ><br>Bone formationTimepoint: This study would be able to compare the efficacy of PRF and Various bone graft material in surgical <br/ ><br>healing of periapical lesion with palatal defects <br/ ><br>It could also act as a pilot study for including PRF <br/ ><br>various Bone Graft material in main stream endo surgical healing <br/ ><br>The evaluation will be done at <br/ ><br>1 3 6 and 12 months after the intervention
Secondary Outcome Measures
NameTimeMethod
ONETimepoint: NOT APPLICABLE
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