To Know the effectiveness of synthetic and bovine derived hydroxyapatite bone graft substitute in the healing of upper front tooth root area of bone.

Active, not recruiting

• Conditions: Inflammatory conditions of jaws, Patients aged between 15-45 yrs of either sex with periapical cyst or residual cyst of anterior maxilla, who required cystectomy and grafting were enrolled in the study. ,

• Registration Number: CTRI/2014/05/004578
• Lead Sponsor: Dr Vivekanand kattimani

Brief Summary

Both bovine derived and synthetic hydroxyapatite graft material are suitable for filling Bone defects, showing less resorption and enhanced bone formation with similar efficacy. However these results were obtained after short duration of follow-up and smaller sample size, but long term studies with large sample size and histomorphometry is recommended for complete evaluation of these grafts.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-05-18
• Last Update Posted: 2021-05-23

Recruitment & Eligibility

• Status: Closed to Recruitment of Participants
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

• Healthy patients with periapical or residual cyst of anterior maxilla diagnosed clinically and radiologically.
• Who requirred cystectomy and grafting .

Exclusion Criteria

• Medically compromised patients.
• Patients with existing metabolic diseases e.g.diabetes.
• Patients with gross mobility due to moderate bone loss.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Enhancement of bone healing	8 weeks

Secondary Outcome Measures

Name	Time	Method
No infection,	Complete bone regeneration

Trial Locations

Locations (1)

department of Oral and Maxillofacial surgery; 🇮🇳 Guntur, ANDHRA PRADESH, India

department of Oral and Maxillofacial surgery

🇮🇳Guntur, ANDHRA PRADESH, India

Dr vivekanand kattimani

Principal investigator

09912400988

drvivekanandsk@gmail.com