Clinical Trials Directory

Trials / Completed

CompletedNCT02507596

Evaluation of Nano-crystalline Hydroxyapatite Silica Gel in Management of Periodontal Intrabony Defects

Clinical and Radiographic Evaluation of Nano-crystalline Hydroxyapatite Silica Gel in the Treatment of Human Periodontal Intrabony Defects

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
35 Years – 50 Years
Healthy volunteers
Accepted

Summary

A clinical and radiographic evaluation of Nano-crystalline hydroxyapatite silica gel in comparison with open flap debridement for management of periodontal intrabony defects.

Detailed description

Thirty patients suffering from advanced chronic periodontitis were included in this randomized controlled clinical trial. Each subject contributed matched two- or three-walled intrabony defects. Patients were equally assigned into the experimental group; Nano-crystalline hydroxyapatite silica gel or the negative control group;open flap debridement. Clinical and radiographic parameters were recorded at baseline and at 3 and 6 months postoperatively.

Conditions

Interventions

TypeNameDescription
BIOLOGICALNano-crystalline hydroxyapatite silica gelit is a type of synthetic bone graft.
PROCEDUREopen flap debridementa periodontal surgical procedure for the purpose of debridement.

Timeline

Start date
2015-04-01
Primary completion
2019-10-01
Completion
2019-12-01
First posted
2015-07-24
Last updated
2022-03-11

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT02507596. Inclusion in this directory is not an endorsement.