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PainPhase 4NCT00318825

Nitrous Oxide for Analgesia During Colonoscopy

A Phase 4 study testing Nitrous oxide in people with Pain, run by Rikshospitalet University Hospital at 1 site in Norway.

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 the study is to determine the analgetic effect of nitrous oxide during colonoscopy, compared to no sedation and intravenous (IV) sedation. Read more about this study

Who is it for?
Ages 18 to 90 years
Conditions the study is for
Pain
What is being tested?
Nitrous oxide
How many people
200 participants
Where
1 siteNorway
Study dates
Apr 2006to Sep 2008
Phase
Phase 4
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 18 to 90 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients referred for colonoscopy

Who cannot join

  • Patients who don't understand information given
  • Age under 18 years
  • Pregnancy
  • Otitis/sinusitis
  • Ileus/bowel obstruction
  • Megacolon
  • Suspected pneumothorax

Trial locations and contacts

1 site in 1 country.

Norway1 site
  • Rikshospitalet University Hospital

    Oslo, 0027

Other trials in Norway

About this study

Official title: Use of Nitrous Oxide for Analgesia During Colonoscopy - A Randomised Trial

The purpose of the study is to determine the analgetic effect of nitrous oxide during colonoscopy, compared to no sedation and intravenous (IV) sedation.

Read the detailed description

Background

Colonoscopy is the gold standard for diagnosis and endoscopic treatment of diseases in the colon and rectum (1). However, many patients experience discomfort during the procedure. Therefore, IV sedation and/or analgesia is routinely given during colonoscopy at the majority of centers around the world.

Midazolam, the most frequent sedative, is a benzodiazepine with hypnotic and sedative effects (2). The half-life of the substance is about 1-2.5 hours, and thus substantially longer than the duration of a colonoscopy (approximately 30 minutes). Additionally, Midazolam gives pronounced amnesia that lasts even longer than the hypnotic effect. Opioids are also frequently used during colonoscopy, with Pethidine as the most common one (half-life: 3 hours).

Use of the above mentioned drugs make it necessary to closely monitor the patients after colonoscopy for several hours, often in specially designed resource-demanding recovery units. Furthermore, due to the amnesia, it is often not possible to give information about findings and further work-up or surveillance to patients after colonoscopy. Finally, patients are not allowed to drive a car for the rest of the day after IV sedation during colonoscopy (2).

Nitrous oxide (N2O) is used as an inhalative gas during anesthesia, labour and at some dentist practices, most frequent in a fixed 50:50 combination with O2. N2O has a strong analgetic effect, and none or only slight sedative effects in concentrations < 80%. N2O has a very rapid onset of effect (a few seconds), and its half-life in the human body after the stop of inhalation is shorter than 1 minute (3). Patients receiving N2O in a 50:50 combination with O2 are awake, don't need post-procedure recovery and may drive their own car home (4). However, as N2O diffuses quickly through biological membranes, caution is warranted when used for patients with the following conditions: sinusitis, otitis, ileus, bowl obstruction, and megacolon. Pregnant women should not be exposed to N2O.

There are some small studies showing good analgetic effects of N2O during colonoscopy, without significant side-effects (5,6,7). One additional study, however, reported on the poor effects of N2O during colonoscopy (8). This study has, however, been subject for critique because it lacks in methodology (9).

N2O is currently used only at some hospitals around the world.

The use of N2O in colonoscopy instead of IV drugs seems to be attractive for several reasons:

  • Adequate analgesia without disturbing sedation during the procedure. The patient is awake and co-operative.
  • No amnesia. All information can be given to the patient immediately after the procedure.
  • The patient can control inhalation of the analgetic N2O himself. This may enhance patient satisfaction.
  • Rapid stop of effect after stopped administration. No surveillance needed, patients can leave the hospital immediately.
  • N2O does not impair psychomotoric abilities (4,10). Thus, patients may use their own car to and from the appointment. This is resource-sparing for the patient and/or payer. Moreover, it may increase compliance for colonoscopy in rural areas.

Hypothesis/endpoint

Primary endpoint:

  • Does the use of N2O during colonoscopy result in adequate analgesia for the patient?

Secondary endpoints

  • Are there any side-effects due to the use of N2O during colonoscopy?
  • Is there a reduction in the number of patients needing IV sedation?
  • Is there any dose reduction of IV drugs?

Methods

The study is a randomised, controlled, double-blinded, single-center trial. Participants, after giving written informed consent, are randomised to one of two treatment groups:

  1. Group 1: N2O inhalation (verum)
  2. Group 2: O2 inhalation (placebo)

All patients in both groups will start their examination without any use of sedatives/analgetics. On demand, the patients will then be instructed to use the mask for inhalation of gas (N2O in verum group, O2 in placebo group). In case of insufficient effect of inhalation, patients in both groups will be given midazolam and/or pethidine until satisfactorily relieved from pain or discomfort.

Both the patient and the endoscopist are blinded with regard to the type of gas used. The endoscopy assistant handles the gas couplings on scene. Randomisation will be done 1:1 for the groups, in blocks of 6 patients, using a computer program and sealed envelopes for concealment on scene.

Study medication

N2O or O2 is to be administrated by inhalation via a mouth/nose mask. N2O and O2 is delivered by the central hospital gas system. The mask contains a tight circle, where gas is only released from the mask by negative pressure from inspiration of the patient. This is to prevent leakage of gas to the environment. The mask is held by the patient and the patient controls the use of the mask (patient-controlled analgesia). The gas system has been approved by the local department of medical equipment. Measurements of N2O concentrations in the endoscopy room are frequently performed by an independent body, in accordance with Norwegian law.

Midazolam (standard dose 2.5 mg) and pethidin (standard dose 25 mg) are used as IV drugs.

Stopping rules

If any adverse effects are observed, blinding is to be broken. The endoscopist decides changes in the sedation procedure, as appropriate in the individual situation.

Measurement of pain and discomfort

After the examination, study participants receive a questionnaire about pain and discomfort during and after the examination. This questionnaire has been used in our department for several years, and is validated for the use in colonoscopy (11, 12). The questionnaire contains a 4-point scale (4-VRS) for the patient's characterisation of pain and discomfort. Additionally, the questionnaire asks about any side-effects observed by the patient.

The questionnaire is to be filled in by the patient at home the day after the procedure, and to be mailed back to the center in a prepaid envelope.

Exclusion criteria:

  1. Patients who don't understand information given
  2. Age under 18 years
  3. Pregnancy
  4. Otitis/sinusitis
  5. Ileus/bowel obstruction
  6. Megacolon
  7. Suspected pneumothorax

Power calculation

As there is only limited knowledge from the literature, we will perform a pilot study including 10 patients in each group. The data of the pilot study will then serve for a power calculation to find out the number of individuals needed in the study.

Ethics

The Norwegian version of the protocol has been approved by the regional ethics committee of Southern Norway (no. S-05225). The Norwegian Data Inspectorate has been informed about the study (no. 25660). The study is registered in a clinical trials registry (www.clinicaltrials.gov).

Ownership and publication

All generated data are owned by Rikshospitalet University Hospital. A manuscript dealing with the data will be submitted to a medical journal for publication, regardless of the nature of the results. Authorship will be according to the Vancouver rules (13).

Literature

  1. Aabakken L. Gastrointestinal endoskopi. Oslo 1997
  2. Felleskatalogen 2004. Felleskatalogen as, Oslo 2004
  3. Forth W, et al. Pharmakologie und Toxikologie. Wissenschaftsverlag. Mannheim 1992
  4. Martin JP, et al. Inhaled patient-administered nitrous oxide/oxygen mixture does not impair driving ability when using as analgesia during screening flexible sigmoidoscopy. Gastrointest Endosc 2000;51:701-3.
  5. Harding TA, et al. The use of inhaled nitrous oxide for flexible sigmoidoscopy: a placebo-controlled trial. Endoscopy 2000;32:457-80
  6. Notini-Gudmarson AK, et al. Nitrous oxide: a valuable alternative for pain relief and sedation during routine colonoscopy Endoscopy 1996;28:283-7
  7. Hedenbro J, et al. Lustgas øverlæget vid koloskopi. Lakartidningen 1996;93:257-8
  8. Forbes GM, Collins BJ. Nitrous oxide for colonoscopy; a randomized controlled study. Gastrointest Endosc 2000;51:271-7.
  9. Faddy SC. Substantial surveillance bias in an unblended study of pain and adverse effects associated with nitrous oxide inhalation or standard medication for colonoscopy. Gastrointest Endosc 2001;54 (letter).
  10. Trojan J, et al. Immediate recovery of psychomotor function after patient-administered nitrous oxide/oxygen inhalation for colonoscopy. Endoscopy 1997;29:17-22
  11. Bretthauer M, et al. A randomized controlled trial to assess the safety and efficacy of carbon dioxide insufflation in colonoscopy. Gut 2002;50:604-7
  12. Skovlund E, et al. Sensitivity of pain rating scales in an endoscopy trial. J Clin Pain, 2005, in press
  13. Uniform requirements for manuscripts submitted to biomedical journals: writing and editing for biomedical
Conditions
Pain
Being tested
Nitrous oxide
Keywords
Pain, Colonoscopy, Sedation
Medical subject headings
Pain

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. Does the use of nitrous oxide (N2O) during colonoscopy result in adequate analgesia for the patient?

Secondary outcomes (3)
  1. Are there any side-effects due to the use of N2O during colonoscopy?

  2. Is there a reduction in the number of patients needing IV sedation?

  3. Is there any dose reduction of IV drugs?

Timeline

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

  1. First posted27 Apr 2006 (estimated)
  2. Study startApr 2006
  3. Primary completionSep 2008
  4. Study completionSep 2008

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 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Single group
Masking
Double blind
Enrolment
200 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00318825
Sponsor's protocol ID
s-05225
Status last verified
Apr 2006
First submitted
25 Apr 2006
Last updated
1 Dec 2010
Results posted
No

Publications

  • Loberg M, Furholm S, Hoff I, Aabakken L, Hoff G, Bretthauer M. Nitrous oxide for analgesia in colonoscopy without sedation. Gastrointest Endosc. 2011 Dec;74(6):1347-53. doi: 10.1016/j.gie.2011.07.071.

    PubMed 22136779

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Nitrous oxide in people with Pain, run by Rikshospitalet University Hospital at 1 site in Norway.

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

Who may be eligible to take part?

The sponsor lists 1 inclusion and 7 exclusion criteria. 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 1 Dec 2010. 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 Norway. 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.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

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?

Does the use of nitrous oxide (N2O) during colonoscopy result in adequate analgesia for the patient?. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00318825, which also lists 1 linked publication.

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 1 Dec 2010.

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