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Dental Extractions in Patients Under Dual Antiplatelet Therapy

NCT02918045 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2019-09-10

No results posted yet for this study

Summary

The purpose of this study is to compare two hemostatic agents in patients under dual antiplatelet therapy using the intraoral bleeding time after dental extractions.

Conditions

  • Blood Coagulation Disorders

Interventions

DEVICE

HemCon Dental Dressing

The Hemcon Dental Dressing is an oral wound dressing made of chitosan.

DEVICE

Oxidized Cellulose Gauze

A common hemostatic measure after dental extractions placed into the extraction socket.

Sponsors & Collaborators

  • University of Sao Paulo General Hospital

    lead OTHER

Principal Investigators

  • Itamara LI Neves, PhD · University of Sao Paulo

  • José C Nicolau, PhD · University of Sao Paulo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-04-11
Primary Completion
2019-07-16
Completion
2019-07-23
FDA Device
Yes

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02918045 on ClinicalTrials.gov