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Analgesia, Patient-controlledPhase 2/3NASKEMINCT01275547

The Analgesic Effect of Combined Treatment With Intranasal S-ketamine and Intranasal Midazolam

A Phase 2/3 study testing s-ketamine & midazolam and Morphine PCA in people with Analgesia, Patient-controlled and Spinal Stenosis, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

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

Introduction Ketamine is an old and generally well accepted analgesic used in the intra- and perioperative setting. Several studies demonstrated the effectiveness of ketamine in the postoperative setting. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
s-ketamine & midazolam and Morphine PCA
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
22 participants
Where
1 siteSwitzerland
Study dates
Jan 2011to Dec 2011
Phase
Phase 2/3
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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Spinal surgery patients with:
  • decompression because of spinal stenosis
  • laminectomy because of spinal stenosis
  • Age > 18 years
  • BMI 18 - 39.9 (kg/m2)

Who cannot join

  • Patients unable to give written informed consent
  • Known drug allergies or intolerance to the study medications morphine, midazolam, ketamine, paracetamol or metamizol
  • Known allergy to crustacea or chitosan
  • Patients using snuff at a regularly basis
  • Recreational drug addiction or abuse
  • Preexisting opioid (tramadol excluded), ketamine or midazolam therapy
Show all 12Show fewer
  • General physical condition ≥ ASA IV
  • Serious intranasal or epipharyngeal problems
  • Mental / psychiatric disorder
  • Pregnancy
  • Patients with renal failure (clearance < 30 ml/min)
  • Patients with liver failure (MELD score > 25) Investigational Product Morphine / S-ketamine / midazolam

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • University Hospital, Basel, Switzerland

    Basel, Canton of Basel-City, 4031

Other trials in Switzerland

About this study

Official title: The Analgesic Effect of Combined Treatment With Intranasal S-Ketamine and Intranasal Midazolam Compared With Morphine Patient Controlled Analgesia in Spinal Surgery Patients

Introduction

Ketamine is an old and generally well accepted analgesic used in the intra- and perioperative setting. Several studies demonstrated the effectiveness of ketamine in the postoperative setting.

Read more

A new formulation of S-ketamine as an intranasal spray device was tested in our hospital in 8 healthy volunteers (unpublished data, EKBB 351/08). 20 mg of S-ketamine were administered intranasally and compared with S-ketamine i.v. and i.m.. None of the volunteers had serious adverse effects or complications. A preliminary data analysis shows a clear analgesic effect and good absorption of the intranasal S-ketamine.

As a next step we would like to investigate the effect of S-ketamine intranasal spray combined with midazolam intranasal spray in a group of postoperative spinal surgery patients. The rational for the combination of intranasal S-ketamine and midazolam is the well known midazolam antagonising effect of ketamine induced psychomimetic adverse effects. Furthermore we know from other studies (EKBB 106/06) that midazolam intranasal spray has relaxant and anxiolytic effects. As far as we know, this is the first study which will examine the combination of S-ketamine and midazolam intranasal sprays in adult patients.

Study work plan

This prospective, randomized, double-blinded non inferiority study will address pain ratings and patient satisfaction in a postoperative setting in two treatment scenarios:

  1. Alternating S-ketamine intranasal unit-dose spray (6 mg per dose) with midazolam intranasal spray (0.75 mg per dose) patient controlled application with a lock-out interval of 20 minutes between two applications and placebo patient controlled analgesia (PCA) with a lock-out interval of 12 minutes with saline 0.9% i.v. for 72 hours or until 40 unit-dose sprays are delivered
  2. PCA with 2 mg morphine with a lock-out interval of 12 minutes i.v. with placebo intranasal spray (saline 0.9% + chitosan) with a minimum lock-out interval of 20 minutes for 72 hours or until 40 unit-dose sprays are delivered

Patient number

We will examine 36 patients, 18 patients in each group. The study duration for an individual patient will be at latest 72 hours, the total study duration is 4 to 5 months.

Study importance

An intranasal spray is an ideal application form for surgery patients, either in- or outpatients. On the other hand, ketamine and S-ketamine is quite often used in the perioperative setting as a rescue analgesic. In higher doses it could be used as an emergency tool in emergency prehospital medicine. In the perioperative setting it is important to evaluate the efficacy and safety of S-ketamine intranasal spray combined with midazolam intranasal spray in patients.

If our study shows that S-ketamine intranasal spray is effective as an analgesic and has good patient acceptance, S-ketamine intranasal spay could be considered as an alternative, completely non-invasive analgesic procedure in a postoperative outpatient setting. As a consequence development of a nasal multidose-applicator combining S-ketamine and midazolam would be of interest.

Being tested
s-ketamine & midazolam, Morphine PCA
Keywords
Patient controlled analgesia, Morphine, S-Ketamine intranasal, Midazolam intranasal
Medical subject headings
Agnosia, Spinal Stenosis

What participants receive

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

  • s-ketamine & midazolamDrug

    s-ketamine 6 mg intranasal midazolam 0.75 mg intranasal

  • Morphine PCADrug

    2 mg Morphine i.v. all 12 minutes as a patient controlled system

Study groups in NCT01275547
Study groupRoleWhat they receive
S-ketamine & midazolam sprayExperimentalall 20 minutes as a patient controlled analgesia alternating s-ketamine / midazolam
Receives: Drug: s-ketamine & midazolam
morphine, patient controlled analgesiaActive comparatormorphine as an active comparator as a patient controlled analgesia system
Receives: Drug: Morphine PCA

What is being measured

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

  1. Numeric rating scale 24 hours after surgery

    NRS after 24 hours after finishing surgery

    Measured: 24 hours

Secondary outcomes (1)
  1. Amount of PCA boli

    Amount of demanded / delivered unit doses of intranasal S-ketamine

    / midazolam or morphine PCA-boli

    Measured: 72 hours

Timeline

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

  1. First posted12 Jan 2011 (estimated)
  2. Study startJan 2011
  3. Primary completionJun 2011
  4. Study completionDec 2011

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 2/3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Care provider
Enrolment
22 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01275547
Sponsor's protocol ID
EKBB28/10
Acronym
NASKEMI
Status last verified
Jan 2013
First submitted
11 Jan 2011
Last updated
29 Jan 2013
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing s-ketamine & midazolam and Morphine PCA in people with Analgesia, Patient-controlled and Spinal Stenosis, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

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 5 inclusion and 12 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 29 Jan 2013. 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 Switzerland. 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 combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

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?

Numeric rating scale 24 hours after surgery (time frame: 24 hours). 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 29 Jan 2013.

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