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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00729261
Other study ID # 1210-04
Secondary ID
Status Completed
Phase Phase 1
First received August 1, 2008
Last updated April 27, 2015
Start date August 2004
Est. completion date May 2006

Study information

Verified date August 2008
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Identifying the optimal time of extubation in a brain injured population should improve patient outcome. Brain injured patients usually remain intubated due to concerns of airway maintenance. Current practice argues that unconscious patients need to remain intubated to protect their airways. More recent data however suggests that delaying extubation in this population increases pneumonias and worsens patient outcomes.

We designed a safety and feasibility study of randomizing brain injured patients into early or delayed extubation. The purpose was to gain insight into patient safety concerns and to obtain estimates of sample size needed for a larger study.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date May 2006
Est. primary completion date May 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Resolution or improvement of any pulmonary process requiring mechanical ventilation.

2. Adequate gas exchange.

3. Adequate ventilation.

4. Respiratory rate to tidal volume ratio <105.

5. Core body temperature < 38 degrees celsius.

6. Hemoglobin > 8 grams per deciliter.

7. No sedative medications for 2 hours.

Neurological requirements included:

1. GCS = 8.

2. Intracranial pressure (ICP) < 15 cm of water and a cerebral perfusion pressure (CPP) > 60 mm Hg for patients with intracranial pressure monitors.

Exclusion Criteria:

1. Age < 18 years.

2. Lack of informed consent by the patients' surrogate.

3. Dependence on mechanical ventilation for at least two weeks prior to enrollment.

4. Patients with tracheostomies.

5. Intubation instituted for therapeutic hyperventilation.

6. Planned surgical or radiological intervention within the next 72 hours.

7. Anticipated neurological or medically worsening conditions (i.e develop cerebral edema or vasospasm).

8. Patients intubated for airway preservation due to airway edema (cervical neck injuries or surgery) as opposed to airway protection.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
extubation
Brian injured patients that remained intubation solely because of a depressed level of consciousness were randomized into immediate extubation or delayed extubation until their level of consciousness improved.All patients met standard ventilatory, and airway criteria for extubation.
continued intubation
patients remain intubated until their Glasgow coma scores improve to greater than 8.

Locations

Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

References & Publications (1)

Coplin WM, Pierson DJ, Cooley KD, Newell DW, Rubenfeld GD. Implications of extubation delay in brain-injured patients meeting standard weaning criteria. Am J Respir Crit Care Med. 2000 May;161(5):1530-6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Modified Rankin Score 6 months No
Secondary nosocomial pneumonias hospital discharge Yes
Secondary reintubations hospital discharge Yes
Secondary ICU length of stay hospital discharge No
Secondary hospital length of stay hospital discharge No
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