Breathing gas may ease pain of cancer procedures
NCT ID NCT00646945
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tested whether a gas mixture called Kalinox (50% nitrous oxide and 50% oxygen) can reduce pain during short invasive procedures in adults with cancer, such as spinal taps or bone biopsies. The trial involved 204 participants and compared Kalinox to a placebo gas (oxygen/nitrogen mix). The main goal was to measure pain using a visual scale and to check for side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Kalinox (50% nitrous oxide / 50% oxygen gas mixture)
- What this could lead to
- If it works, this could provide a simple, fast-acting pain relief option for cancer patients undergoing short, painful procedures.
- What could go wrong
- This is a completed phase 4 trial, so results are already known. The gas may cause side effects like nausea or dizziness, and it may not work better than standard pain relief or a placebo.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
204 people
The number who actually took part.
- Start date
-
Sep 2007
- Finished
-
Oct 2008
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age \> 18 year * OMS between 0 to 3 * Patient who has to undergo an invasive gesture or a painful care * Absence of contra-indication to the administration of the product Exclusion Criteria: * Patient already included in another incompatible study with this protocol * Patient incapable of self-assessment by the EVA * Confusional syndrome * OMS \> 3 * Patient already included in this protocol * Exclusion criteria linked to the product
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Centre Alexis Vautrin
Vandœuvre-lès-Nancy, 54 500, France
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