Comparison of Three Types of Sutures in Oral Surgery. Study of Bacterial Colonization, Tissue Reaction and Clinical Characteristics: Randomized Clinical Study

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversidad de Granada

About this trial

Considering the wide variety of surgical sutures currently marketed in the field of Dentistry, it was decided to conduct a study comparing the microbial adhesion and antibacterial activity of three different types of sutures used in Oral Surgery (Silk, non-absorbable polyamide monofilament and non-absorbable expanded polytetrafluoroethylene).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with indication for extraction of a third lower molar retained in an unfavorable position that requires a bayonet incision in the surgical procedure.

Age: patients aged 18 years or older.

ASA I patients (Classification of the American Society of Anesthesiology, 1979): healthy patients who tolerate stress well, without systemic pathology, no anxiety and in whom a therapeutic modification is not necessary.

Disqualifiers

Pregnant or breastfeeding women.

Smoking patients.

Trial design

Design model

Single group

Treatments tested in this trial

  • To Compare 3 different suture materials used in oral surgery

    Other intervention

    To compare bacterial colonization, tissue reaction and clinical characteristics such as wound healing and patient postoperative outcomes in 3 different suture materials used in oral surgery.

Treatment groups

24 Participants
are divided into 3 treatment groups
Group A: Suture 1: Silk.Other 1 intervention
Group B: Suture 2: Non-absorbable polyamide monofilament.Other 1 intervention
Group C: Suture 3: Non-resorbable expanded polytetrafluoroethylene.Other 1 intervention

Trial outcomes

Primary outcomes

1

Bacterial colonization

Microbiological analysis: CFU and qPCR bacterial count.

Time frame
7 days.
2

Level of inflammation

The degree of soft tissue inflammation was assessed using Visual Analogue Scale (VAS).

Time frame
7 days.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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