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Diaphragmatic Pacemaker in Tetraplegic Patients With Spinal Cord Injuries

Primary Purpose

Respiratory Paralysis, Diaphragmatic Paralysis, Spinal Cord Injury

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
NeuRx RA/4 diaphragmatic pacemaker
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Paralysis

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years old or more
  • Cervical spinal cord injuries patients under mechanical ventilation
  • Clinically stable after spinal cord injury
  • Clinical acceptable bilateral phrenic nerve function demonstrated with electromyography and neural conduction time
  • Fluoroscopic visible diaphragmatic movements under stimulation
  • Hemodynamically stable
  • No co-morbidities that can interfere with pacemaker implantation or function
  • Pregnancy negative test for women
  • Patient or legal representative informed consent

Exclusion Criteria:

  • Active pulmonary disease
  • Active cardiovascular disease
  • Active cerebral disease
  • Hemodynamic instability or low oxygen levels in ambient air
  • Hospitalization for infection in the last 3 months
  • Significant scoliosis or chest disease
  • Obesity
  • Poor compliance to the protocol from the patient or the caregiver

Sites / Locations

  • Heart Institute (InCor) Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo
  • Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

NeuRx

Arm Description

Outcomes

Primary Outcome Measures

Volume comparison of the basal with the tidal volume obtained with the NeuRx RA/4 pacemaker in patients with diaphragmatic paralysis
The ability of the NeuRx RA / 4 to obtain clinically acceptable tidal volume during a period of 4 continuous hours will be evaluated by spirometry. Clinically acceptable volume is defined as a volume in excess of 15% above the basal metabolic requirements of the particular patient. For a male patient, the flow volume to meet the basal metabolic requirement is set at 7 ml/kg body weight, while for a female patient, it is defined in 6ml/Kg body weight.

Secondary Outcome Measures

Functional rehabilitation by measure of total usage time, both day and night
Using spreadsheets to patients and caregivers, will collect information related to the use of the device, such as total usage time, the preference to use it both day and night instead of a mechanical ventilator, or to use it partial time to perform any activity or acquire independence that would otherwise be difficult with mechanical ventilation.

Full Information

First Posted
June 23, 2011
Last Updated
March 18, 2013
Sponsor
University of Sao Paulo
Collaborators
Synapse Biomedical
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1. Study Identification

Unique Protocol Identification Number
NCT01385384
Brief Title
Diaphragmatic Pacemaker in Tetraplegic Patients With Spinal Cord Injuries
Official Title
Evaluation of the NeuRx RA/4 Diaphragmatic Pacemaker in Tetraplegic Patients With Spinal Cord Injuries in Ventilator Support
Study Type
Interventional

2. Study Status

Record Verification Date
March 2013
Overall Recruitment Status
Completed
Study Start Date
June 2011 (undefined)
Primary Completion Date
November 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo
Collaborators
Synapse Biomedical

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Permanent dependency of breathing apparatus due to spinal cord injury is traditionally treated with different types of mechanical ventilation. However, the electric ventilation became a possibility through their most current versions, such as diaphragmatic pacemakers. Diaphragmatic pacemakers rhythmically stimulates the diaphragm to replace the functions of the respiratory center that doesn't works well or is inaccessible. However, this modality has the prerequisite that the phrenic nerve and diaphragm muscle are normal. The reason for the development of diaphragmatic pacemaker freeing the patient from the ventilator. By using the mechanical energy of the diaphragm of the patient, the patient may come not need the ventilator tubing, tracheostomy, and with the help of their caregivers, the inconvenient mechanical ventilators.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Paralysis, Diaphragmatic Paralysis, Spinal Cord Injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NeuRx
Arm Type
Other
Intervention Type
Device
Intervention Name(s)
NeuRx RA/4 diaphragmatic pacemaker
Intervention Description
Patients will be implanted with 4 intramuscular electrodes, 2 in each hemi-diaphragm, using laparoscopic techniques. The abdominal cavity is inflated with CO2 and 4 ports are inserted: one for optics, 2 for a probe containing a temporary electrode for mapping the diaphragm and the electrode insertion tool, and a smaller one for the output wires of the electrodes of the abdominal cavity. The intra-abdominal pressure variation during the stimulation test (mapping) will be measured externally by one of the ports. Sites that provide the optimal response (greater region and magnitude) are noted. Once the optimal site for electrode placement is identified two intramuscular electrodes are deployed in each hemi-diaphragm. The guide wires will come out of the peritoneum through the port placed in the xiphoid region. An additional electrode is placed subcutaneously in the upper abdomen. The instruments and ports are then removed and the incision sites closed.
Primary Outcome Measure Information:
Title
Volume comparison of the basal with the tidal volume obtained with the NeuRx RA/4 pacemaker in patients with diaphragmatic paralysis
Description
The ability of the NeuRx RA / 4 to obtain clinically acceptable tidal volume during a period of 4 continuous hours will be evaluated by spirometry. Clinically acceptable volume is defined as a volume in excess of 15% above the basal metabolic requirements of the particular patient. For a male patient, the flow volume to meet the basal metabolic requirement is set at 7 ml/kg body weight, while for a female patient, it is defined in 6ml/Kg body weight.
Time Frame
One year
Secondary Outcome Measure Information:
Title
Functional rehabilitation by measure of total usage time, both day and night
Description
Using spreadsheets to patients and caregivers, will collect information related to the use of the device, such as total usage time, the preference to use it both day and night instead of a mechanical ventilator, or to use it partial time to perform any activity or acquire independence that would otherwise be difficult with mechanical ventilation.
Time Frame
One year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years old or more Cervical spinal cord injuries patients under mechanical ventilation Clinically stable after spinal cord injury Clinical acceptable bilateral phrenic nerve function demonstrated with electromyography and neural conduction time Fluoroscopic visible diaphragmatic movements under stimulation Hemodynamically stable No co-morbidities that can interfere with pacemaker implantation or function Pregnancy negative test for women Patient or legal representative informed consent Exclusion Criteria: Active pulmonary disease Active cardiovascular disease Active cerebral disease Hemodynamic instability or low oxygen levels in ambient air Hospitalization for infection in the last 3 months Significant scoliosis or chest disease Obesity Poor compliance to the protocol from the patient or the caregiver
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fabio B Jatene, MD, PhD
Organizational Affiliation
Thoracic Surgery Department, Heart Institute (InCor) do Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Manuel J Teixeira, MD, PhD
Organizational Affiliation
Neurosurgery Department, Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Miguel L Tedde, MD, PhD
Organizational Affiliation
Thoracic Surgery Department, Heart Institute (InCor) do Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Heart Institute (InCor) Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo
City
Sao Paulo
State/Province
SP
Country
Brazil
Facility Name
Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo
City
Sao Paulo
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
23184201
Citation
Tedde ML, Vasconcelos Filho P, Hajjar LA, de Almeida JP, Flora GF, Okumura EM, Osawa EA, Fukushima JT, Teixeira MJ, Galas FR, Jatene FB, Auler JO Jr. Diaphragmatic pacing stimulation in spinal cord injury: anesthetic and perioperative management. Clinics (Sao Paulo). 2012 Nov;67(11):1265-9. doi: 10.6061/clinics/2012(11)07.
Results Reference
result
PubMed Identifier
23147048
Citation
Tedde ML, Onders RP, Teixeira MJ, Lage SG, Ballester G, Brotto MW, Okumura EM, Jatene FB. Electric ventilation: indications for and technical aspects of diaphragm pacing stimulation surgical implantation. J Bras Pneumol. 2012 Sep-Oct;38(5):566-72. doi: 10.1590/s1806-37132012000500005. English, Portuguese.
Results Reference
result

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Diaphragmatic Pacemaker in Tetraplegic Patients With Spinal Cord Injuries

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