Trial record 8 of 143 for:    carbon monoxide

Safety Study of Inhaling Carbon Monoxide in Healthy Volunteers

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01050933
Recruitment Status : Terminated (resident left and no one to take over)
First Posted : January 18, 2010
Last Update Posted : November 17, 2015
The Physicians' Services Incorporated Foundation
Information provided by (Responsible Party):
Dr. Paul Belliveau, Queen's University

Brief Summary:

Post operative ileus (POI), a temporary paralysis of the intestines, is a serious health care problem. It normally occurs in all patients after surgery to the abdomen but in some cases can result in serious complications. The objective of this study is to determine if inhaling very low doses of carbon monoxide (CO) before and after colon surgery will shorten the duration of normal POI and/or prevent the development of POI complications in patients undergoing colon surgery.

This preliminary study will be conducted in ten healthy volunteers to monitor for blood levels and adverse effects that occur at different durations of exposure of inhaled CO to establish a safe dose for patients in the main trial. For the main trial, patients requiring surgery to their colon will be assigned randomly to receive one hour treatments of either CO or oxygen by face mask before and after their operation.

We hypothesize that healthy volunteers will be able to tolerate 1 hour doses of 250 ppm of CO with minimal side effects. It is also anticipated that for each dose of CO administered, the blood levels of CO will remain well under poisonous levels. Finally, we anticipate blood levels of CO will return to baseline level within 24 hours following the last dose of CO.

Condition or disease Intervention/treatment Phase
Healthy Drug: 250 ppm carbon monoxide Phase 1

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 10 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Safety and Tolerability of Inhaled Carbon Monoxide in Healthy Volunteers
Study Start Date : September 2010
Actual Primary Completion Date : June 2011
Actual Study Completion Date : October 2011

Arm Intervention/treatment
Experimental: Carbon Monoxide
Healthy volunteers will receive 250 ppm of carbon monoxide by face mask. This dose will be administered for 1 hour with continuous COHb monitoring. At baseline and at each half hour time point, a blood sample will be drawn to be analyzed by the gas chromatograph. After 1 hour, the volunteer will be excused and asked to return in 4 hours and this procedure repeated. At any point, if the COHb level reaches 10%, administration of CO will be terminated.
Drug: 250 ppm carbon monoxide
250 ppm of inhaled carbon monoxide over one hour

Primary Outcome Measures :
  1. Adverse Event Rate [ Time Frame: Before and after carbon monoxide exposure ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Men and women, age > 18 years.
  • Women must be using acceptable contraceptives, post-menopausal or surgically sterile.
  • No prior smoking history.
  • BMI between 16 and 30 inclusive.
  • In good health as per medical history, physical exam, vital signs & ECG.

Exclusion Criteria:

  • Exposure to carbon monoxide during the 48 hours prior to the study day.
  • Occupational exposure to CO.
  • Significant disease that may put the volunteer at risk because of participation in the study or may influence the results of the study or the volunteer's ability to participate in the study.
  • Baseline blood level of COHb >2%.
  • Patients with underlying lung disease such as asthma or COPD.
  • Baseline oxygen saturation <92% on room air.
  • Planned pregnancy, already pregnant or breastfeeding.
  • Participation in another clinical trial within 2 months prior to study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01050933

Canada, Ontario
Kingston General Hospital
Kingston, Ontario, Canada
Sponsors and Collaborators
Queen's University
The Physicians' Services Incorporated Foundation
Principal Investigator: Paul Belliveau, MD Queen's University

Responsible Party: Dr. Paul Belliveau, Principal Investigator, Queen's University Identifier: NCT01050933     History of Changes
Other Study ID Numbers: POICO-A
First Posted: January 18, 2010    Key Record Dates
Last Update Posted: November 17, 2015
Last Verified: November 2015

Keywords provided by Dr. Paul Belliveau, Queen's University:
Healthy volunteer

Additional relevant MeSH terms:
Carbon Monoxide
Molecular Mechanisms of Pharmacological Action
Neurotransmitter Agents
Physiological Effects of Drugs