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Role of Anabolic Steroids on Intensive Care Unit-Acquired Weakness (RAS-ICU)

Primary Purpose

Critical Illness Polyneuropathies

Status
Unknown status
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
Testosterone cypionate
Standard nutrition and physical therapy at ICU
Sponsored by
Hospital de Clinicas de Porto Alegre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Illness Polyneuropathies focused on measuring prolonged mechanical ventilation, critically ill patients, anabolic steroid

Eligibility Criteria

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

Inclusion Criteria:

  • Individuals older than 18 years
  • Mechanical ventilation by orotracheal tube for more than 14 consecutive days
  • Mechanical ventilation by tracheostomy for more than 8 consecutive days

Exclusion Criteria:

  • End of life care
  • Known hypersensitivity to formula
  • Venous or arterial thrombosis within last 6 months: ischemic stroke, myocardial infarction, acute peripheral arterial occlusion, acute mesenteric ischemia, deep venous thromboembolism, pulmonary embolism
  • Decompensated congestive heart failure
  • Acute liver failure or acute on chronic liver failure
  • Refractory shock (norepinephrine dose >0.3 mcg/kg/min or equivalent doses of any vasoactive agent)
  • Platelets below <20,000 / mm3 without transfusion plan
  • Personal history of prostate cancer
  • Primary neuromuscular disorders such as myasthenia gravis, Guillain-Barré syndrome, amyotrophic lateral sclerosis, Duchenne Muscular dystrophy
  • Current or prior spinal cord injury

Sites / Locations

  • Hospital de Clínicas de Porto AlegreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Anabolic patients

Control

Arm Description

Intramuscular injection of testosterone cypionate 200mg every 15 days in addition to standard nutrition and physical therapy at ICU.

Standard nutrition and physical therapy at ICU without administration of testosterone cypionate

Outcomes

Primary Outcome Measures

Mechanical ventilation dependence
Days of any positive pressure ventilation described in the patient record from the start of the study

Secondary Outcome Measures

Muscle weakness
The muscle weakness measured weekly by the study team through the Medical Research Council (MRC)
Ultrasound diaphragm
Weekly the study team will perform diaphragm ultrasound to monitor the respiratory muscles, observing measures of inspiration and expiration.
ICU length of stay
Patient's length of stay in the intensive care unit after the start of the study as described in the patient record
Hospital length of stay
Period of stay of the patient in the hospital after discharge from the intensive care unit described in the patient record

Full Information

First Posted
January 31, 2017
Last Updated
January 31, 2017
Sponsor
Hospital de Clinicas de Porto Alegre
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1. Study Identification

Unique Protocol Identification Number
NCT03038919
Brief Title
Role of Anabolic Steroids on Intensive Care Unit-Acquired Weakness
Acronym
RAS-ICU
Official Title
Pilot Randomized, Controlled Trial of Testosterone Therapy in Chronic Critically Ill Patients and Its Potential Effects on Weaning From Mechanical Ventilation and Intensive Care Unit-acquired Weakness
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Unknown status
Study Start Date
October 2016 (undefined)
Primary Completion Date
October 2017 (Anticipated)
Study Completion Date
January 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital de Clinicas de Porto Alegre

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The researchers intend to investigate possible anabolic effects of bi-weekly exogenous testosterone administration during intensive care unit (ICU) stay for up to 8 weeks. Control group will receive standard ICU management and will also be followed during ICU stay.
Detailed Description
For the study chronic critical patients will be included according to criterion of mechanical ventilation by orotracheal tube> 14 consecutive days or mechanical ventilation by tracheostomy> 8 consecutive days and that do not present exclusion criteria. Patients will be randomized into two follow-up groups: Intervention group with anabolic steroid and control group. The anabolic steroid intervention group will receive a bi-weekly dose of 200mg intramuscular testosterone cypionate and receive the standard treatment of nutritional therapy and physical therapy. While patients in the control group will receive only the standard treatment of nutrition and physical therapy, without addition of the anabolic drug. At the beginning of the study and weekly the patients will be evaluated in relation to the muscular profile with diaphragm ultrasound and Medical Research Council (MRC) application. In addition to the collection of serum homograms, leukogram, lipid profile and renal function tests. Weight and nutritional therapy-related data will be identified in the patient's chart regarding caloric and protein requirement and supply adequacy. In the inclusion and biweekly will be collected serum levels of free testosterone, blood count, leukogram, blood gas, renal function and liver function. Nitrogen balance of patients from urinary urea will be performed. The evaluations of the groups and the intervention with the anabolic steroid will be of 8 weeks or during the period of dependence of the mechanical ventilation. After this period the patients will be monitored for the outcome: length of stay in the intensive care unit, hospital stay until discharge and clinical outcome: death or discharge.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness Polyneuropathies
Keywords
prolonged mechanical ventilation, critically ill patients, anabolic steroid

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Anabolic patients
Arm Type
Experimental
Arm Description
Intramuscular injection of testosterone cypionate 200mg every 15 days in addition to standard nutrition and physical therapy at ICU.
Arm Title
Control
Arm Type
Other
Arm Description
Standard nutrition and physical therapy at ICU without administration of testosterone cypionate
Intervention Type
Drug
Intervention Name(s)
Testosterone cypionate
Other Intervention Name(s)
testosterone
Intervention Description
Bi-weekly intramuscular injection of testosterone cypionate 200mg.
Intervention Type
Other
Intervention Name(s)
Standard nutrition and physical therapy at ICU
Intervention Description
follow-up of the patient without use of testosterone cypionate
Primary Outcome Measure Information:
Title
Mechanical ventilation dependence
Description
Days of any positive pressure ventilation described in the patient record from the start of the study
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Muscle weakness
Description
The muscle weakness measured weekly by the study team through the Medical Research Council (MRC)
Time Frame
8 weeks
Title
Ultrasound diaphragm
Description
Weekly the study team will perform diaphragm ultrasound to monitor the respiratory muscles, observing measures of inspiration and expiration.
Time Frame
8 weeks
Title
ICU length of stay
Description
Patient's length of stay in the intensive care unit after the start of the study as described in the patient record
Time Frame
9 months
Title
Hospital length of stay
Description
Period of stay of the patient in the hospital after discharge from the intensive care unit described in the patient record
Time Frame
9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Individuals older than 18 years Mechanical ventilation by orotracheal tube for more than 14 consecutive days Mechanical ventilation by tracheostomy for more than 8 consecutive days Exclusion Criteria: End of life care Known hypersensitivity to formula Venous or arterial thrombosis within last 6 months: ischemic stroke, myocardial infarction, acute peripheral arterial occlusion, acute mesenteric ischemia, deep venous thromboembolism, pulmonary embolism Decompensated congestive heart failure Acute liver failure or acute on chronic liver failure Refractory shock (norepinephrine dose >0.3 mcg/kg/min or equivalent doses of any vasoactive agent) Platelets below <20,000 / mm3 without transfusion plan Personal history of prostate cancer Primary neuromuscular disorders such as myasthenia gravis, Guillain-Barré syndrome, amyotrophic lateral sclerosis, Duchenne Muscular dystrophy Current or prior spinal cord injury
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sara C Rosa
Phone
+5551997381047
Email
sararosa92@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ana Carolina P Antonio, PhD
Phone
+5551984428820
Email
ana.carolina.antonio@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Silvia RR Vieira, PhD
Organizational Affiliation
Hospital de Clínicas de Porto Alegre - RS
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de Clínicas de Porto Alegre
City
Porto Alegre
State/Province
RS
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ana Carolina P Antonio, PhD
Phone
+555133598000
Ext
8637
Email
aantonio@hcpa.edu.br
First Name & Middle Initial & Last Name & Degree
Sara C Rosa
Phone
+555133598000
Ext
8637
Email
sararosa92@gmail.com
First Name & Middle Initial & Last Name & Degree
Sara C da Rosa
First Name & Middle Initial & Last Name & Degree
Ana Carolina P Antonio, PhD
First Name & Middle Initial & Last Name & Degree
Silvia RR Vieira, PhD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Role of Anabolic Steroids on Intensive Care Unit-Acquired Weakness

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