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Clinical Evaluation of Sutures in Periodontal Surgery

Completed
Conditions
Periodontal Debridement
Interventions
Procedure: Periodontal resective surgery
Registration Number
NCT02013661
Lead Sponsor
Universitat Internacional de Catalunya
Brief 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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Qualification for the study was based on the need for resective periodontal surgery (apically positioned flap and osseous recontouring) at four or more consecutive interproximal sites per quadrant
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Exclusion Criteria
  • systemic diseases, such as diabetes, chronic obstructive pulmonary disease, or an immunologic disease that would affect wound healing; allergies to prescribed medication; and/or current pregnancy or breast feeding were excluded from the study
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Suture in Periodontal resective surgeryPeriodontal resective surgeryFour types of suture including silk, polypropylene, PGA, and PTFE
Primary Outcome Measures
NameTimeMethod
presence or absence of Suture looseningseven days after surgery

Seven days after the surgical procedure, the surgeon assessed suture loosening; recording loose or not Loose

Secondary Outcome Measures
NameTimeMethod
presence and level of erythema and edema.seven days after surgery

Seven days after the surgical procedure a blind researcher clinically evaluated erythema and edema. Adding a score related to a gingival index

Trial Locations

Locations (1)

Universitat Internacional de Catalunya

🇪🇸

San Cugat del Valles, Barcelona, Spain

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