Sedation and Physiological Effects of Intranasal Dexmedetomidine in Severe COPD

COPD Clinical Trial

Official title:

Sedation and Physiological Effects of Intranasal Dexmedetomidine in Severe COPD

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02211118
• Other study ID #: Nystrom01
• Status: Completed
• Phase: Phase 4
• Start date: October 2014
• Est. completion date: April 2016

Study information

• Verified date: July 2019
• Source: Dayton VA Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A variety of medications have been used to treat the anxiety, discomfort, and fear associated with continuous and sudden episodic breathlessness in patients with advanced respiratory disease. Opioids and benzodiazepines, used alone or in combination, are commonly prescribed for this distressing symptom. Clinicians are concerned about the adverse effects of opioids, especially respiratory depression, so they frequently prescribe benzodiazepines. Recent studies have shown that benzodiazepine use is associated with increased adverse respiratory outcomes in older adults with Chronic Obstructive Pulmonary Disease (COPD).

Dexmedetomidine may be an alternative to current drug therapies for breathlessness. Dexmedetomidine produces a dose dependent sedation, anxiolysis, and analgesia without respiratory depression or cognitive dysfunction. The drug can be administered intranasally to induce light to moderate sedation of several hours duration.

The objective of the proposed research, a pilot study, is to assess the dose dependent safety and efficacy of intranasal dexmedetomidine in clinically stable patients with severe COPD. This will be accomplished in a staffed acute care setting with routine vital signs monitoring and pulse oximetry. Patients will be assessed objectively and subjectively for their level of sedation by validated sedation scales.

This pilot study is an initial investigation of a drug with favorable pharmacologic properties in this patient population with distressing and difficult to treat symptoms. The pilot study may provide evidence that a larger trial is needed to confirm the study results, or evidence that additional study in symptomatic patients and treatment comparison trials should be pursued.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: April 2016
• Est. primary completion date: October 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 45 Years to 70 Years

Eligibility

Inclusion Criteria:

• Severe COPD (FEV1 30-50% predicted)

• Age 45-70

• American Society of Anesthesiologists (ASA) Class 3

• Body Mass Index <35 kg/meter squared

• No prior history of adverse reactions to alpha 2 agonists (dexmedetomidine, clonidine)

• Women of non-child bearing age

Exclusion Criteria:

• known adverse reaction, allergy or hypersensitivity, to alpha 2 agonists

• not nothing by mouth (NPO)

• ASA class >3

• Home oxygen therapy >2LPM by nasal cannula continuous use

• Any evidence of nasal mucosal inflammation, irritation, bleeding or ulceration

• Pregnancy, or possibility of pregnancy

• Coronary heart disease with stable or unstable angina

• Baseline heart rate <55 beats per minute

• Bradyarrhythmia, heart block, presence of pacemaker

• Congestive Heart Failure or known Cardiomyopathy (Ejection Fraction <40% by ECHO, MUGA, or myocardial perfusion imaging)

• Cor pulmonale

• Liver disease (hepatic transaminases above the upper limit of normal, cirrhosis, end stage liver disease)

• diagnosis of moderate to severe Obstructive Sleep Apnea

• currently enrolled in any other research study involving drugs or devices

Related Conditions & MeSH terms

• COPD
• Dexmedetomidine
• Sedation

Intervention

Drug:
• Intranasal dexemdetomidine (IN-DEX)

Locations

Country	Name	City	State
United States	Dayton VA Medical Center	Dayton	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
Dayton VA Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Modified Observer's Assessment of Alertness/Sedation Scale		every 15 minutes up to 5 hours after intranasal desmedetomidine
Primary	Sedation Visual Analog Scale (VAS)		Every 15 minutes up to 5 hours after intranasal dexemdetomidine
Primary	Changes in Vital Signs	Heart rate, noninvasive blood pressure, respitory rate, pulse oximetry	Every 5 minutes for 90 minutes, then every 15 minutes for up to 5 hours