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Hemodynamic and Electrocardiographic Effects of Hyaluronidase Associated With Local Anaesthetics

Primary Purpose

Cardiac Arrhythmias

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
3.6mL 2% Mepivacaine with 1:100,000 epinephrine
Lower Third Molar Extraction
Hyaluronidase
Placebo
Sponsored by
Mauricio Jose Tornelli
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Arrhythmias focused on measuring Local Anaesthetics, Mepivacaine, hyaluronoglucosaminidase, Hemodynamic, Electrocardiography and Dentistry.

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients should present bilateral lower third molars (teeth 38 and 48) for extraction and identical anatomical arrangement;
  • Absence of significant clinical morbidities, ASA I (American Society of Anesthesiologists, 1963);
  • Aged over 18 years.

Exclusion Criteria:

  • Women during pregnancy or lactation;
  • Smokers;
  • History of sensitivity to any drug used in the research;
  • Presence or history of cancer or an infectious lesion;
  • Individuals who used any medication in the last 15 days (except oral contraceptives);
  • Presence of abscess or pericoronitis in the region to be operated;
  • Patients who required supplemental anaesthesia upon anaesthetic block of the inferior alveolar nerve (post-randomisation exclusion).

Sites / Locations

  • Stomatology Department, FOUSP

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Hyaluronidase

Placebo

Arm Description

Lower Third Molar Extraction -- 3.6mL 2% Mepivacaine with 1:100,000 epinephrine + Hyaluronidase

Lower Third Molar Extraction -- Anesthetic: 3.6 mL of the LA 2% HCl mepivacaine with 1:100,000 epinephrine + Placebo (0.9% saline)

Outcomes

Primary Outcome Measures

Arrhythmia
Atrial or ventricular arrhythmias: isolated, paired or clustered extrasystoles, tachycardia, bradycardia and fibrillation.

Secondary Outcome Measures

PR segment
• Duration of the PR segment, in milliseconds.
QRS complex
• Duration of the QRS complex, in milliseconds.
Change from baseline Heart rate
• Change from baseline Heart rate (evaluated period - baseline), in beats per minute. Values will be expressed as the absolute difference and the percentage of change.
Corrected QT
• Duration of the calculated corrected QT segment (QTc) in milliseconds.
Heart rate (absolute values)
• Heart rate, (absolute values) in beats per minute.

Full Information

First Posted
October 3, 2012
Last Updated
October 31, 2012
Sponsor
Mauricio Jose Tornelli
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
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1. Study Identification

Unique Protocol Identification Number
NCT01719978
Brief Title
Hemodynamic and Electrocardiographic Effects of Hyaluronidase Associated With Local Anaesthetics
Official Title
Hemodynamic and Electrocardiographic Effects of Hyaluronidase Associated With Local Anaesthetics: a Double-blind "Split-mouth" Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
October 2007 (undefined)
Primary Completion Date
October 2007 (Actual)
Study Completion Date
December 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Mauricio Jose Tornelli
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Among the adjuvants to local anaesthetics (LA), the enzyme hyaluronidase is most often used as a diffuser agent of the LA in ophthalmic anaesthesia. It serves to improve clinical efficacy and prolong anaesthesia as an alternative to long-lasting and potentially more dangerous LA, especially in patients with increased cardiovascular risk. There is scarce clinical data about the safety of the use of hyaluronidase in dental procedures. This study aimed to compare hemodynamic and electrocardiographic variables during a dental surgical procedure using a local anaesthetic associated with hyaluronidase or placebo in healthy subjects.
Detailed Description
This double-blind crossover "split-mouth" trial evaluated the cardiovascular effects induced by 3.6 mL of the LA 2% HCl mepivacaine with 1:100,000 epinephrine, concomitantly with 75 TRU/mL hyaluronidase or placebo in inferior alveolar nerve block, for the performance of bilateral and symmetrical third molar surgery in 20 outpatients. Cardiovascular parameters, including systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rate (HR), were monitored using oscillometric and photoplethysmographic methods in 10 clinical stages. Electrocardiographic records (ECG) of 12 leads were obtained in four steps. Hyaluronidase injected concomitantly with LA did not induce changes in SBP, DBP and HR compared to placebo. There were no instances of ST segment depression, ST segment elevation, wide QRS complex extrasystoles, or narrow QRS complex extrasystoles. To date, few studies in dentistry have investigated the effects of local anaesthetic efficacy in hyaluronidase, and even fewer have studied the relation to systemic effects induced by this interaction. The use of LA injected concomitantly with 75 TRU/mL of hyaluronidase is safe when using this dose and route of administration. Clinical Relevance: In dentistry, few studies have investigated the effects of hyaluronidase on local anaesthetic efficacy, and even fewer have examined the possible systemic effects induced by this interaction.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrhythmias
Keywords
Local Anaesthetics, Mepivacaine, hyaluronoglucosaminidase, Hemodynamic, Electrocardiography and Dentistry.

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
ParticipantInvestigator
Allocation
Non-Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hyaluronidase
Arm Type
Active Comparator
Arm Description
Lower Third Molar Extraction -- 3.6mL 2% Mepivacaine with 1:100,000 epinephrine + Hyaluronidase
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Lower Third Molar Extraction -- Anesthetic: 3.6 mL of the LA 2% HCl mepivacaine with 1:100,000 epinephrine + Placebo (0.9% saline)
Intervention Type
Drug
Intervention Name(s)
3.6mL 2% Mepivacaine with 1:100,000 epinephrine
Other Intervention Name(s)
Mepivacaine with epinephrine
Intervention Description
Local anesthetic with vasoconstrictor
Intervention Type
Procedure
Intervention Name(s)
Lower Third Molar Extraction
Other Intervention Name(s)
Molar surgery
Intervention Description
Lower Third Molar Extraction with LA + hyaluronidase (or placebo)
Intervention Type
Drug
Intervention Name(s)
Hyaluronidase
Intervention Description
75RTU Hyaluronidase administration concomitant to the local anesthetic
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Saline, 0.9% NaCl
Intervention Description
1mL 0.9% saline administration concomitant to the local anesthetic
Primary Outcome Measure Information:
Title
Arrhythmia
Description
Atrial or ventricular arrhythmias: isolated, paired or clustered extrasystoles, tachycardia, bradycardia and fibrillation.
Time Frame
5min before anaesthesia
Secondary Outcome Measure Information:
Title
PR segment
Description
• Duration of the PR segment, in milliseconds.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
QRS complex
Description
• Duration of the QRS complex, in milliseconds.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
Change from baseline Heart rate
Description
• Change from baseline Heart rate (evaluated period - baseline), in beats per minute. Values will be expressed as the absolute difference and the percentage of change.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
Corrected QT
Description
• Duration of the calculated corrected QT segment (QTc) in milliseconds.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
Heart rate (absolute values)
Description
• Heart rate, (absolute values) in beats per minute.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Other Pre-specified Outcome Measures:
Title
Systolic Pressure (absolute values)
Description
Systolic Blood Pressure (absolute values), in mmHg.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
Diastolic Pressure (absolute values)
Description
Diastolic Blood Pressure, in mmHg.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
Mean Blood Pressure (absolute values)
Description
Mean Blood Pressure, in mmHg.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
Change from baseline Diastolic Pressure
Description
• Change from baseline Diastolic Blood Pressure (evaluated period - baseline), in mmHg. Values will be expressed as the absolute difference and the percentage of change.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
Change from baseline Systolic Pressure
Description
• Change from baseline Systolic Blood Pressure (evaluated period - baseline), in mmHg. Values will be expressed as the absolute difference and the percentage of change.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day
Title
Change from baseline Mean Arterial Blood Pressure
Description
• Change from baseline Mean Arterial Blood Pressure (evaluated period - baseline), in mmHg. Values will be expressed as the absolute difference and the percentage of change.
Time Frame
5min before anaesthesia; During anaesthetic injection; 5min after anaesthesia; Incision; Syndesmotomy; Luxation; Avulsion; Curetage; Suture; 1 hour after the end of surgery (At Patient discharge) and in the 7th postoperative day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients should present bilateral lower third molars (teeth 38 and 48) for extraction and identical anatomical arrangement; Absence of significant clinical morbidities, ASA I (American Society of Anesthesiologists, 1963); Aged over 18 years. Exclusion Criteria: Women during pregnancy or lactation; Smokers; History of sensitivity to any drug used in the research; Presence or history of cancer or an infectious lesion; Individuals who used any medication in the last 15 days (except oral contraceptives); Presence of abscess or pericoronitis in the region to be operated; Patients who required supplemental anaesthesia upon anaesthetic block of the inferior alveolar nerve (post-randomisation exclusion).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gustavo F Prado, PhD
Organizational Affiliation
FMUSP
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Maria A Borsatti, PhD
Organizational Affiliation
FOUSP
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Rodney G Rocha, PhD
Organizational Affiliation
FOUSP
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Helena R Tornelli, MD, S
Organizational Affiliation
FOUSP
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Renata MS Prado, MS, S
Organizational Affiliation
FOUSP
Official's Role
Study Chair
Facility Information:
Facility Name
Stomatology Department, FOUSP
City
Sao Paulo
ZIP/Postal Code
05508-000
Country
Brazil

12. IPD Sharing Statement

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Hemodynamic and Electrocardiographic Effects of Hyaluronidase Associated With Local Anaesthetics

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