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Opioid-Related DisordersNCT00000260

Effects of Behavioral Contingencies on Effects of Nitrous Oxide - 12

A study testing Nitrous oxide in people with Opioid-Related Disorders and Substance-Related Disorders, run by University of Chicago at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to conduct experiments to examine subjective and reinforcing effects of nitrous oxide. Mood altering and psychomotor effects will be tested on non-drug abusers and preference procedures will be used to assess reinforcing effects. Read more about this study

Who is it for?
Ages 21 years and olderHealthy volunteers can take part
What is being tested?
Nitrous oxide
How many people
18 participants
Where
1 siteUnited States
Study dates
Jun 1997to Jan 1998
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Please contact site for information.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Chicago, Anesthesia & Critical Care

    Chicago, Illinois, 60637

Other trials in United States

About this study

Official title: Effects of Behavioral Contingencies on Effects of Nitrous Oxide

The purpose of this study is to conduct experiments to examine subjective and reinforcing effects of nitrous oxide. Mood altering and psychomotor effects will be tested on non-drug abusers and preference procedures will be used to assess reinforcing effects. Comparisons between nitrous oxide, opiates, and benzodiazepine antagonists will be made. To examine the effects of different behavioral contingencies in modulating the reinforcing effects of nitrous oxide in healthy volunteers.

Being tested
Nitrous oxide
Keywords
nitrous oxide, subjective effects, reinforcer, inhalant, healthy volunteer
Medical subject headings
Opioid-Related Disorders, Substance-Related Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nitrous oxideDrug

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mood

  2. Choice of nitrous oxide vs placebo

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Sep 1999 (estimated)
  2. Study startJun 1997
  3. Primary completionJan 1998
  4. Study completionJan 1998

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Enrolment
18 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00000260
Sponsor's protocol ID
NIDA-08391-12
Other IDs
R01DA008391, R01-08391-12
Status last verified
May 2015
First submitted
20 Sep 1999
Last updated
27 May 2015
Results posted
No

Questions about this trial

What is this clinical trial studying?

A study testing Nitrous oxide in people with Opioid-Related Disorders and Substance-Related Disorders, run by University of Chicago at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 May 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mood. The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 May 2015.

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