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Randomized Clinical Trial With Aminocaproic Acid in the Prevention of Exodontic Bleeding in Anticoagulants Patients

Primary Purpose

Oral Hemorrhage

Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Aminocaproic acid
Routine dental care
lidocaine and epinephrine
Paracetamol
Sponsored by
Grupo de Estudos Multicentricos em Onco-Hematologia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Oral Hemorrhage focused on measuring anticoagulation, extraction, epsilon amino caproic

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients over 18 years of age, use of warfarin sodium with or without anti-platelet aggregation, indicating simple extractions whose INR values are between 2.0 and 4.0 and that consent to participate in the study.

Exclusion Criteria:

  • Patients with platelet count < 50,000 / mm3 Pregnant women or lactating Patients with hypersensitivity to the components of EACA. Patients with coagulopathies Patients who have impacted teeth, ankylosed or root morphological alterations that may complicate the procedure Patients who fail to submit laboratory and radiographic examinations necessary for the surgery

Sites / Locations

  • Clementino Fraga Filho University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

aminocaproic acid

Routine care after dental extraction

Arm Description

Crushed tablets inserted in the dental socket post-extraction

Chompret´s manoeuver, suture, surgical wound compression with gauze for 20 minutes

Outcomes

Primary Outcome Measures

bleeding post-exodontic
No bleeding Bleeding Light - blood in saliva Moderate Bleeding - bleeding controlled with local measures Severe Bleeding - when required surgical intervention and / or hospitalization

Secondary Outcome Measures

Full Information

First Posted
September 10, 2014
Last Updated
September 11, 2014
Sponsor
Grupo de Estudos Multicentricos em Onco-Hematologia
Collaborators
Rio de Janeiro State Research Supporting Foundation (FAPERJ)
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1. Study Identification

Unique Protocol Identification Number
NCT02238288
Brief Title
Randomized Clinical Trial With Aminocaproic Acid in the Prevention of Exodontic Bleeding in Anticoagulants Patients
Official Title
Randomized Clinical Trial to Verify the Effectiveness of Topical Aminocaproic Acid in the Prevention of Post-exodontic Bleeding in Patients on Anticoagulants
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Unknown status
Study Start Date
December 2013 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
July 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Grupo de Estudos Multicentricos em Onco-Hematologia
Collaborators
Rio de Janeiro State Research Supporting Foundation (FAPERJ)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients using anticoagulants present an increased risk of bleeding when subjected to oral surgery. Suspending or reducing the oral anticoagulant dose to perform invasive procedures, may result in thromboembolic events, putting patients health in risk. Recent studies advocate the dental surgery treatment without suspending the anticoagulant therapy, since the values of the international normalized ratio (INR) are in acceptable therapeutic levels and local measurements are taken for the hemostasis control. The aim of this study is to compare the effectiveness use of intra-alveolar epsilon amino caproic acid (EACA) associated to daily rinses with the drug, with routine post-surgical procedures, to control the post-exodontic bleeding in anticoagulated patients. Patients will be referred by the anticoagulation clinic of the Clementino Fraga Filho University Hospital. Once the study criteria is met patients will be randomly allocated into two groups and subsequently subjected to clinical and periodontal examination, radiographic examination and pre-operative periodontal therapy. Laboratory tests (partial thromboplastic time, prothrombin time, international normalized ratio and platelet count) will be held on the day of the extraction. Patients in group 1 ( EACA ) will receive a paste composed of 01 macerated EACA tablet (500 mg), mixed with 0.9% saline solution in the alveolar socket, and routine post-operative care. Additionally, patients will perform oral rinses three times a day, on the first two post-operative days, with a solution from the macerated EACA 500mg tablet diluted in 2 spoons of filtered water. Patients allocated in group 2 (control) will receive routine post-operative care. Classification of immediate bleeding will be held by the professional, on the day of the surgery, immediately after the suture and twenty minutes later and the delayed bleeding, recorded by the patient through a daily questionnaire. The Statistical Package for the Social Sciences (SPSS)© (IBM, Chicago, USA) 20.0 is used as the database and the Chi-square, Kruskal-Wallis and Mann-Whitney tests will be applied to statistical analysis of the results.The study was approved by the ethical and research committee of the Clementino Fraga Filho University Hospital . All patients will sign a free consent and informed term.
Detailed Description
All patients will be submitted to clinical and radiographic examination. Once selected, patients will receive hygiene instruction and will be submitted to full mouth scaling one week before the procedure with an ultrasonic device (CavitronR - Dentsply). The random allocation of patients will obey the order obtained in the computerized program Allocation 1.0 Software© (Isfahan, Iran, 2004). All patients should have the prothrombin time (PT) and INR, active thromboplastin partial time (aTPT) and platelet counts tests on the day of surgery. Patients who present INR< 2.0 e > 4 will be assessed by the medical team about the possibility of change in the dose of medication to the surgical procedure. Patients with predisposing heart conditions the bacterial endocarditis will receive antibiotic prophylaxis as recommendations from American Association of Cardiology (AHA) of 2007. All extraction procedures will be performed by non-traumatic conventional surgical techniques, under local anesthesia (2% lidocaine and epinephrine 1: 100,000). Just one extraction will be performed in each surgical procedure, by the same surgeon. All patients will receive digital compression of socket with sterile gauze for 5 minutes (Chompret 's manoeuver) and suture with non-resorbable wire, silk 3.0 type . Everyone will receive the base analgesic prescription Paracetamol 750 mg (Tylenol© - Johnson & Johnson), 01 tablet every 6 hours, by oral administration, for control of postoperative pain. Patients are divided into two groups: Group 1 (EACA) - patients will receive the intra-alveolar application of a 500 mg tablet of the epsilon-amino caproic acid (EACA - Ipsilon® - Nikko Brazil, RJ) crushed in 0.9% saline. Additionally, they will be instructed to rinse with 500mg EACA tablets macerated and diluted in 2 tablespoons of water three times a day, in the two days after the extraction. Group 2 (control) - patients will receive routine postoperative care. Classification of Bleeding will be performed by the professional on the day of surgery at two times: one time (immediately after extraction) and time 2 (after 20 minutes). The bleeding will be classified as follows: No bleeding Light bleeding - blood in saliva Moderate Bleeding - bleeding controlled with local measures Severe Bleeding - when surgical intervention is required Late bleeding will be recorded by the patient through daily questionnaire. The bleeding will be classified as follows: No bleeding Blood stained saliva Bleeding that stopped after compression bandage and ice pack for 20 minutes Bleeding stopped only after professional intervention

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oral Hemorrhage
Keywords
anticoagulation, extraction, epsilon amino caproic

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
154 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
aminocaproic acid
Arm Type
Active Comparator
Arm Description
Crushed tablets inserted in the dental socket post-extraction
Arm Title
Routine care after dental extraction
Arm Type
Other
Arm Description
Chompret´s manoeuver, suture, surgical wound compression with gauze for 20 minutes
Intervention Type
Drug
Intervention Name(s)
Aminocaproic acid
Other Intervention Name(s)
Ipsilon©
Intervention Description
Crushed tablet in the dental socket
Intervention Type
Other
Intervention Name(s)
Routine dental care
Other Intervention Name(s)
Routine procedures after dental extractions
Intervention Description
Chompret´s manoeuver, suture, surgical wound compression with gauze for 20 minutes
Intervention Type
Drug
Intervention Name(s)
lidocaine and epinephrine
Intervention Description
2%
Intervention Type
Drug
Intervention Name(s)
Paracetamol
Intervention Description
750 mg
Primary Outcome Measure Information:
Title
bleeding post-exodontic
Description
No bleeding Bleeding Light - blood in saliva Moderate Bleeding - bleeding controlled with local measures Severe Bleeding - when required surgical intervention and / or hospitalization
Time Frame
up to twenty minutes

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients over 18 years of age, use of warfarin sodium with or without anti-platelet aggregation, indicating simple extractions whose INR values are between 2.0 and 4.0 and that consent to participate in the study. Exclusion Criteria: Patients with platelet count < 50,000 / mm3 Pregnant women or lactating Patients with hypersensitivity to the components of EACA. Patients with coagulopathies Patients who have impacted teeth, ankylosed or root morphological alterations that may complicate the procedure Patients who fail to submit laboratory and radiographic examinations necessary for the surgery
Facility Information:
Facility Name
Clementino Fraga Filho University Hospital
City
Rio de Janeiro
State/Province
RJ
ZIP/Postal Code
21864-440
Country
Brazil

12. IPD Sharing Statement

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Randomized Clinical Trial With Aminocaproic Acid in the Prevention of Exodontic Bleeding in Anticoagulants Patients

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