Page last updated: 2024-11-07

entonox

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Entonox, also known as nitrous oxide and oxygen (N2O/O2), is a premixed medical gas that is commonly used as an analgesic for pain relief. It is a 50:50 mixture of nitrous oxide (N2O) and oxygen (O2). Nitrous oxide is a colorless, odorless gas that is often used as a recreational drug, but it is also used in medicine as an anesthetic and analgesic. Oxygen is a colorless, odorless gas that is essential for life. Entonox is administered by inhalation through a mask or nasal cannula. It is a rapid-acting analgesic that provides pain relief within seconds. The effects of entonox usually last for 3-5 minutes. Entonox is widely used in healthcare settings, including hospitals, clinics, and emergency departments. It is used to relieve pain from a variety of conditions, including childbirth, dental procedures, and minor injuries. The use of Entonox is particularly common in childbirth, where it is used to relieve pain during labor and delivery. Entonox is also used in the treatment of acute pain, such as pain from burns and fractures. The use of Entonox is generally safe, but it can cause some side effects, such as dizziness, nausea, and vomiting. Entonox is typically not recommended for people with certain medical conditions, such as certain lung diseases or heart problems. '

Entonox: combination drug containing premixed 50% nitrous oxide (dinitrogen oxide) & 50% oxygen [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID108123
MeSH IDM0041239

Synonyms (10)

Synonym
eutonal
nitronox
anesoxyn-50
entonox
nitralgin
nitrogen oxide (n2o), mixt. with oxygen
54510-89-3
kalinox
kalinox 170 bar
molecular oxygen;nitrous oxide

Research Excerpts

Overview

Entonox is a 50 : 50 combination of nitrous oxide and oxygen, which may be used to manage pain during colonoscopy. Some women are interested in continuous breathing in face mask.

ExcerptReferenceRelevance
"Entonox (N2O2) which is an inhalational gas for relieving labor pain is commonly used intermittently; however some women are interested in continuous breathing in face mask. "( Effects of continuous use of Entonox in comparison with intermittent method on obstetric outcomes: a randomized clinical trial.
Agah, J; Baghani, R; Safiabadi Tali, SH; Tabarraei, Y, 2014
)
2.14
"Entonox is a 50 : 50 combination of nitrous oxide and oxygen, which may be used to manage pain during colonoscopy. "( A randomized controlled trial comparing continuous and as-required nitrous oxide use during screening colonoscopy.
Ball, AJ; Din, S; Donnelly, M; Riley, SA, 2015
)
1.86

Effects

ExcerptReferenceRelevance
"Entonox has been used effectively in different specialties for pain relief. "( Use of inhaled nitrous oxide for minor eyelid surgery: a placebo-controlled study.
Bhatt, R; Child, V; Johns, S; Kurli, M; Musadiq, M; Sandramouli, S; Stott, M, 2003
)
1.76

Toxicity

ExcerptReferenceRelevance
" Success (completion of planned treatment), cooperation (modified Venham scale), and adverse events were recorded."( A clinical trial of efficacy and safety of inhalation sedation with a 50% nitrous oxide/oxygen premix (Kalinox™) in general practice.
Collado, V; Faulks, D; Hennequin, M; Koscielny, S; Nicolas, E; Onody, P, 2012
)
0.38

Bioavailability

ExcerptReferenceRelevance
"Fentanyl is a potent opioid that is well absorbed via the oral mucosa."( Oral transmucosal fentanyl citrate versus placebo for painful dressing changes: a crossover trial.
Barker, L; Larsen, D; MacIntyre, PA; Margetts, L, 2007
)
0.34
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (117)

TimeframeStudies, This Drug (%)All Drugs %
pre-199024 (20.51)18.7374
1990's23 (19.66)18.2507
2000's46 (39.32)29.6817
2010's18 (15.38)24.3611
2020's6 (5.13)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 72.96

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index72.96 (24.57)
Research Supply Index5.12 (2.92)
Research Growth Index4.58 (4.65)
Search Engine Demand Index125.55 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (72.96)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials43 (34.68%)5.53%
Reviews11 (8.87%)6.00%
Case Studies11 (8.87%)4.05%
Observational1 (0.81%)0.25%
Other58 (46.77%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (7)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Analgesia of Acute Coronary Syndromes With ST-segment Elevation in a Pre-hospital Setting. Randomized Non-inferiority Trial of the Association MEOPA + Paracetamol Versus Morphine. [NCT02198378]Phase 4680 participants (Actual)Interventional2014-11-30Completed
Optimizing the Use of Entonox® During Screening Colonoscopy: an Open Randomised Controlled Trial [NCT01865721]Phase 4100 participants (Actual)Interventional2013-01-31Completed
The Effect of Entonox on Stages of Labor in Nulliparous Women :a Randomized Controlled Trial [NCT04321642]80 participants (Actual)Interventional2019-11-01Completed
Effect of Nitrous Oxide in Treating Neuropathic Pain: A Pilot Study in Chronic Low Back Pain Patients [NCT01172600]78 participants (Actual)Interventional2011-01-31Completed
A Single-centre, Randomised Controlled Study of Entonox Versus Midazolam Sedation in Gastroscopy. [NCT01744184]Phase 4200 participants (Anticipated)Interventional2013-05-31Recruiting
Inhaled Nitrous Oxide and Labor Analgesia [NCT01738672]Phase 216 participants (Actual)Interventional2012-02-29Terminated
Comparison of the Role of Epidural Analgesia Versus Non-epidural Analgesia in Postnatal Depression and Persistent Pain Development: a Randomized Controlled Trial [NCT03167905]Phase 2/Phase 3881 participants (Actual)Interventional2017-06-15Active, not recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT01172600 (12) [back to overview]Change in Oswestry Score (% of Disability) From Baseline to 2nd Block
NCT01172600 (12) [back to overview]Change in Oswestry Score (% of Disability) From Baseline to 3 Months Follow-up
NCT01172600 (12) [back to overview]Change in Oswestry Score (% of Disability) From Baseline to 3rd Block
NCT01172600 (12) [back to overview]Change in VAS Pain Score From Baseline to 3 Month Follow-up
NCT01172600 (12) [back to overview]Change in VAS Pain Score From Baseline to Before 2nd Block
NCT01172600 (12) [back to overview]Change in VAS Pain Score From Baseline to Before 3rd Block
NCT01172600 (12) [back to overview]Usage of Opioid
NCT01172600 (12) [back to overview]Usage of Opioid
NCT01172600 (12) [back to overview]Usage of Opioids
NCT01172600 (12) [back to overview]Biomarkers
NCT01172600 (12) [back to overview]Biomarkers
NCT01172600 (12) [back to overview]Biomarkers
NCT01738672 (6) [back to overview]Crossover To Epidural
NCT01738672 (6) [back to overview]Emesis
NCT01738672 (6) [back to overview]Participant Satisfaction
NCT01738672 (6) [back to overview]Anxiety
NCT01738672 (6) [back to overview]Labor Pain
NCT01738672 (6) [back to overview]Nausea

Change in Oswestry Score (% of Disability) From Baseline to 2nd Block

Oswestry score ranges from 0% to 100%, which measures % of disability. The outcome is change in the Oswestry score from baseline (before 1st block) to before 2nd block. (NCT01172600)
Timeframe: At baseline (before 1st block) and before the 2nd block, typically at 1 month from baseline

Interventionabsolute percentage (Mean)
Entonox-7
Oxygen-6

[back to top]

Change in Oswestry Score (% of Disability) From Baseline to 3 Months Follow-up

Oswestry score ranges from 0% to 100%, which measures % of disability. The outcome is change in the Oswestry score from baseline (before 1st block) to 3 months follow-up. (NCT01172600)
Timeframe: At baseline (before 1st block) and 3 months follow-up after last block (maximum of 3 blocks with a typical 1 month interval between blocks)

Interventionabsolute percentage (Mean)
Entonox-11
Oxygen-6

[back to top]

Change in Oswestry Score (% of Disability) From Baseline to 3rd Block

Oswestry score ranges from 0% to 100%, which measures % of disability. The outcome is change in the Oswestry score from baseline (before 1st block) to before 3rd block. (NCT01172600)
Timeframe: At baseline (before 1st block) and before the 3rd block, typically at 2 months from baseline

Interventionabsolute percentage (Mean)
Entonox-10
Oxygen-7

[back to top]

Change in VAS Pain Score From Baseline to 3 Month Follow-up

"10-cm-long Visual Analog Scale (VAS) pain score, ranges from 0 (no pain) to 10 (worst pain imaginable). It was measured before 1st 2nd and 3rd block and at 3 month follow-up.~The primary outcome was the change in VAS pain score from baseline (before 1st block) to the 3 month follow-up." (NCT01172600)
Timeframe: At baseline (before 1st block) and 3 months follow-up after last block (maximum of 3 blocks with a typical 1 month interval between blocks)

Interventionunits on a scale (Mean)
Entonox-1.6
Oxygen-1.2

[back to top]

Change in VAS Pain Score From Baseline to Before 2nd Block

"10-cm-long Visual Analog Scale (VAS) pain score, ranges from 0 (no pain) to 10 (worst pain imaginable). It was measured before 1st 2nd and 3rd block and at 3 month follow-up.~The primary outcome was the change in VAS pain score from baseline (before 1st block) to before the 2nd block." (NCT01172600)
Timeframe: At baseline (before 1st block) and before the 2nd block, typically at 1 month from baseline

Interventionunits on a scale (Mean)
Entonox-0.6
Oxygen-0.4

[back to top]

Change in VAS Pain Score From Baseline to Before 3rd Block

"10-cm-long Visual Analog Scale (VAS) pain score, ranges from 0 (no pain) to 10 (worst pain imaginable). It was measured before 1st 2nd and 3rd block and at 3 month follow-up.~The primary outcome was the change in VAS pain score from baseline (before 1st block) to before the 3rd block" (NCT01172600)
Timeframe: At baseline (before 1st block) and before the 3rd block, typically at 2 months from baseline

Interventionunits on a scale (Mean)
Entonox-2.1
Oxygen-0.5

[back to top]

Usage of Opioid

(NCT01172600)
Timeframe: 3 months follow-up after last block (maximum of 3 blocks with a typical 1 month interval between blocks)

Interventionparticipants (Number)
Entonox6
Oxygen9

[back to top]

Usage of Opioid

(NCT01172600)
Timeframe: 3rd block, typically at 2 months from baseline

Interventionparticipants (Number)
Entonox3
Oxygen2

[back to top]

Usage of Opioids

(NCT01172600)
Timeframe: 2nd block, typically at 1 month from baseline

Interventionparticipants (Number)
Entonox3
Oxygen7

[back to top]

Biomarkers

BIOMARKERS: IL-1β, IL-6, IL-10, 1L-17A, IFN-γ, and TNF-α (NCT01172600)
Timeframe: baseline - before 1st block

,
Interventionpg/ml (Median)
IL-1βIL-6IL-10IL-17AIFN-γTNF-α
Entonox2062261741469313
Oxygen140198176137859

[back to top]

Biomarkers

BIOMARKERS: IL-1β, IL-6, IL-10, 1L-17A, IFN-γ, and TNF-α (NCT01172600)
Timeframe: before 2nd block, typically at 1 month from baseline

,
Interventionpg/ml (Median)
IL-1βIL-6IL-10IL-17AIFN-γTNF-α
Entonox12822414214612410
Oxygen1001271631287910

[back to top]

Biomarkers

BIOMARKERS: IL-1β, IL-6, IL-10, 1L-17A, IFN-γ, and TNF-α (NCT01172600)
Timeframe: before 3rd block, typically at 2 months from baseline

,
Interventionpg/ml (Median)
IL-1βIL-6IL-10IL-17AIFN-γTNF-α
Entonox120110170153975
Oxygen1132392441408811

[back to top]

Crossover To Epidural

Participants crossing over from nitrous oxide to epidural. (NCT01738672)
Timeframe: Initiation of nitrous oxide to completion of delivery.

Interventionparticipants (Number)
Nitrous Oxide8

[back to top]

Emesis

Participant reported emesis (yes or no). (NCT01738672)
Timeframe: During administration of nitrous oxide

Interventionparticipants experiencing emesis (Number)
Nitrous Oxide1

[back to top]

Participant Satisfaction

Participant reported score of satisfaction with nitrous oxide for labor analgesia, using a numerical rating scale (NRS) ranging from completely dissatisfied (0) to completely satisfied (100). (NCT01738672)
Timeframe: 24 hours after delivery

Interventionunits on a scale (Median)
Nitrous Oxide90

[back to top]

Anxiety

Participant reported anxiety score, using a numerical rating scale (NRS) ranging from no anxiety (0) to severe anxiety (10). (NCT01738672)
Timeframe: At baseline, and at 1 hour after initiation of nitrous oxide

Interventionunits on a scale (Mean)
Baseline1 hour after initiation of nitrous oxide
Nitrous Oxide2.502.00

[back to top]

Labor Pain

Participant reported pain score, using a numerical rating scale (NRS) ranging from no pain (0) to severe pain (10). (NCT01738672)
Timeframe: At baseline, and at 1 hour after initiation of nitrous oxide

Interventionunits on a scale (Mean)
Baseline1 hour after initiation of nitrous oxide
Nitrous Oxide8.888.18

[back to top]

Nausea

Participant reported nausea score, using a numerical rating scale (NRS) ranging from no nausea (0) to severe nausea (10). (NCT01738672)
Timeframe: At baseline, and at 1 hour after initiation of nitrous oxide

Interventionunits on a scale (Mean)
Baseline1 hour after initiation of nitrous oxide
Nitrous Oxide0.250.46

[back to top]