Long-term Clinical Study Evaluating the Safety and Efficacy of Dexmedetomidine in ICU Subjects

• Status: Completed
• Trial end date: 2008-06-01
• Target enrollment: 0
• Participant gender: All

Summary

Evaluate efficacy and safety of dexmedetomidine long term administration in ICU patients who require more than 24 hours sedation.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Hospira, Inc.; Hospira, now a wholly owned subsidiary of Pfizer
• Collaborator: Maruishi Pharmaceutical
• Treatments: Dexmedetomidine

Criteria

Inclusion Criteria:

1. Patient or legally acceptable representative (if acceptable by Institutional Review Board/Ethics Committee) has signed and dated the Informed Consent after the study had been fully explained.

2. Patient is male or female, at least 20 years of age.

3. In case of surgical ICU patient, who is in condition of American Society of Anesthesiologists (ASA) I to III Class preoperatively.

4. Patient is on mechanical ventilation and anticipated to require sedation more than 24 hours following a surgery.

5. If patient is female with child bearing potential, she is to be non-pregnant, and not lactating.

Exclusion Criteria:

1. Patient has serious central nervous system (CNS) trauma.

2. Patient requires the use of neuromuscular blocking agents after admission to ICU, except for the insertion of the endotracheal tube.

3. Patient is hospitalized for drug overdose within the last 30 days.

4. Patient in whom alpha-2 antagonists or alpha-2 agonists are contraindicated.

5. Patient is currently being treated or has been treated within the last 30 days with alpha-2 agonist or antagonist.

6. Patient has participated in a trial with any experimental drug within 30 days prior to admission to the ICU.

7. Terminally ill patient, whose life duration expectancy is no more or around 30 days.

8. Patient is considered unable to undergo any procedure required by the protocol.

9. Patient with excessive bleeding which will likely require surgery.

10. In the Investigator's opinion, patient has any symptom or factor, which might increase risk to the patient or preclude obtaining satisfactory study data.