Clinical Trials Directory

Trials / Completed

CompletedNCT02013661

Clinical Evaluation of Sutures in Periodontal Surgery

Clinical Evaluation of Four Types of Suture in Periodontal Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
40 (actual)
Sponsor
Universitat Internacional de Catalunya · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The aims of this study were to evaluate and compare tissue erythema, edema and knot loosening among four types of suture one week after periodontal surgery.

Detailed description

Forty patients participated in this prospective, randomized, double-blind clinical trial. Vertical mattress sutures were used following resective periodontal surgery performed by one operator. Four suture materials were selected for evaluation: 5-0 silk; 5-0 polypropylene; 5-0 polyglycolic acid (PGA), and 4-0 polytetrafluoroethylene (PTFE). Seven days after the surgical procedure, the surgeon assessed suture loosening and removed the sutures. A blind researcher clinically evaluated erythema and edema.

Conditions

Interventions

TypeNameDescription
PROCEDUREPeriodontal resective surgerysurgical periodontal debridement is performed after periodontal phase I

Timeline

Start date
2011-06-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2013-12-17
Last updated
2013-12-17

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT02013661. Inclusion in this directory is not an endorsement.