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CancerKETACANCERNCT04459234

Prospective Multicentre Study of the Use of Ketamine in the Treatment of Refractory Chronic Pain in the French CLCC

An observational study of Cancer and Chronic Pain, run by Centre Leon Berard at 12 sites in France.

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 primary objective of this study is to describe the administration practices of the antalgic Ketamine in French CLCC (Centre de Lutte Contre le Cancer) in terms of indication (neuropathic sequelae pains, morphine additional effect or morphine withdrawal, intensity, localisation…) and administration protocol (route… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Cancer, Chronic Pain, Neuropathic Pain
What is being tested?
Ketamine use in CLCC sites (indication and administration protocol)
How many people
81 participants
Where
12 sitesFrance
Study dates
2 Feb 2021to 9 Mar 2023
Phase
Observational
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

Study population: This is a prospective, multicentre study, considered as " non-RIPH (Recherche n'Impliquant pas la Personne Humaine ". Indeed, the patient's participation in the study and the completion of the various questionnaires has no impact on patient's safety and is not likely to change his/her management. The treatment will be conducted according to the standard practices of each participating site (continuous or discontinuous protocol, dosage, rhythm of administration, monitoring, etc.). The questionnaires and scales used in this study are part of the recommended tools for monitoring this population.

Who may be able to join

  • Patient at least 18 years old at the day of consenting to the study
  • Patient followed for a solid tumour or a hematological malignancy (treated or under treatment)
  • Patient presenting cancer chronic pain or post cancer treatment pain
  • Patient followed by a CLCC's intractable chronic pain consultation or centre
  • Patient with an indication of 1st Ketamine course:
  • Analgesic treatment of cancer chronic pain
Show all 11Show fewer
  • Analgesic treatment for a post-cancer treatment chronic pain
  • Help for withdrawal from opioid treatment prescribed for a chronic cancer pain
  • Patient not previously treated by Ketamine
  • Patient covered by a medical insurance
  • Patient and/or family did not decline data collection after complete information (information sheet)

Who cannot join

  • Patient presenting chronic pains not related to cancer or its treatments
  • Patient with a proven psychotic history
  • Patient who is not fluent enough in French

Trial locations and contacts

12 sites in 1 country.

12 sites in 1 country

France12 sites
  • Institut Bergonié

    Bordeaux, 33076

  • Centre François Baclesse

    Caen

  • Centre Jean Perrin

    Clermont-Ferrand, 63011

  • Centre Leon Berard

    Lyon, 69008

  • Institut Paoli Calmettes

    Marseille, 13273

  • Institut de Cancérologie de Montpellier

    Montpellier, 34298

  • Institut Curie

    Paris, 75005

  • Institut Godinot

    Reims, 51056

  • Centre Eugène Marquis

    Rennes, 35042

  • Institut Universitaire du Cancer (IUCT)

    Toulouse, 31059

  • Institut de Cancérologie de Lorraine Alexis Vautrin

    Vandœuvre-lès-Nancy, 54519

  • Institut Gustave Roussy

    Villejuif, 94805

Other trials in France

About this study

Official title: KETACANCER: Prospective Multicentre Study of the Use of Ketamine in the Treatment of Refractory Chronic Pain in the French CLCC

The primary objective of this study is to describe the administration practices of the antalgic Ketamine in French CLCC (Centre de Lutte Contre le Cancer) in terms of indication (neuropathic sequelae pains, morphine additional effect or morphine withdrawal, intensity, localisation…) and administration protocol (route, posology, duration, administration sequence, premedication).

The secondary objectives are to evaluate in the context of cancer, the analgesic efficacy, the tolerance profile (biological and clinical toxicities) and the quality of life, including anxiety and depression.

In addition, the described parameters will be evaluated as safety and efficacy predictive factors of the Ketamine in oncology.

Read the detailed description

Almost 382,000 new cancers have been diagnosed in France in 2018. Regular progresses in their management have improved the overall survival of patients, sometimes with sequelae that may be particularly painful. Thus for 20 to 45% of patients treated for breast cancer, pain persists 5 years later.

If remission is a regularly reached target, cancer was also the cause of 157,000 deaths in 2018 in France, preceded by months or years of progression of a chronic disease that regularly causes pain. Pain during cancer (chronic cancer pain for CIM-11) remains a frequent symptom, and its prevalence has slightly changed during the last 20 years.

In the European EPIC study, carried out in 2006, 76% of the cancer patients (and 62% of French patients) presented moderate to severe pains linked to cancer, daily for more than half of them.

Even when identified, chronic cancer pain is still under-treated in 25 to 60% of cases worldwide, including in the most developed countries.

When well-managed, pain's management now allows the relief of almost 80% of patients. Pain's management is based in particular on a precise and adapted use of the different opioids through different routes of administration (oral, transdermal, trans-mucosal, parenteral, etc.).

A neuropathic component of pain exists in almost a third of cases and may require specific treatments when opioids are insufficient. In all cases, the treatment is integrated into a multidisciplinary management, in connection with the ongoing oncological treatments, the loco-regional treatments available (radiotherapy, interventional radiology, etc.) and with an adapted psychosocial management.

Ketamine is an NMDA receptor antagonist (N-Methyl-D-Aspartate) indicated as a high dose anesthetic. It is used in the context of peri-operative pain for its anti-hyperalgesic properties. These properties have led to its use also in palliative care (outside the marketing authorization [AMM]) to treat hyperalgesia linked to the use of high-doses of opioids, as well as depression. For non-cancer pains, ketamine is widely used by centres and consultations specialized in refractory chronic pain management in different pains not relieved by standard treatments: neuropathic pain, fibromyalgia, etc., or even in opioids weaning aid.

The bibliographic data are not homogeneous and of low quality. Despite the weakness of the available data, ketamine is widely used in France in chronic pain in situation of therapeutic impasse. The protocols used vary according to the prescribers and services practices: venous route in general, sometimes subcutaneous or even oral; doses varying from 30 to 200 mg / day, infusion duration varying from a few hours to several days, discontinuous administration by cycle or continuous administration, etc.

Current knowledge is too limited in oncology to have a consensus on the use of ketamine :

  • Often retrospective studies with heterogeneous treatment protocols;
  • Studied populations also heterogeneous, with insufficiently documented indications;
  • Staff not able to answer adequately the questions raised. This situation largely explains the heterogeneity of the Ketamine practices of use in oncology

It is essential to draw up an inventory of the ketamine use by the French CLCCs pain teams and to identify the profile of patients in whom i) the treatment is ineffective and must be avoided regarding toxicities ii) the potential efficacy required further investigations. Built on a methodology close to the OKAPI study, the KETACANCER study will enable to compare indirectly the results of the two studies.

To do this, it is proposed to conduct the KETACANCER prospective study in a precise population defined a priori, and corresponding to the following indications:

  • Neuropathic sequelae pain
  • Additional effect of morphine
  • Morphine weaning.
Being tested
Ketamine use in CLCC sites (indication and administration protocol)
Keywords
Cancer, Palliative care, Ketamine, Chronic pain
Medical subject headings
Neoplasms, Chronic Pain, Neuralgia

What participants receive

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

  • Ketamine use in CLCC sites (indication and administration protocol)Drug

    Collection of information concerning Ketamine use by French CLCCs pain teams (first prescription):

    1. Indications : analgesic treatment of cancer chronic pain, analgesic treatment for a post-cancer treatment chronic pain, help for withdrawal from opioid treatment prescribed for a chronic cancer pain
    2. Administration protocol: route, posology, duration, administration sequence, premedication
    3. Antalgic efficacy
    4. Tolerance profile
    5. Quality of life, anxiety and depression evaluations

What is being measured

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

  1. Describe the administration practices of the antalgic Ketamine in French CLCC (Centre de Lutte Contre le Cancer) in terms of indication

    neuropathic sequelae pains, morphine additional effect or morphine withdrawal, intensity, localisation

    Measured: Up to 3 months after inclusion

  2. Describe the administration practices of the antalgic Ketamine in French CLCC (Centre de Lutte Contre le Cancer) in terms of administration protocol

    route, posology, duration, administration sequence, premedication

    Measured: Up to 3 months after inclusion

Secondary outcomes (6)
  1. Evaluate in the context of cancer the antalgic efficacy

    Questionnaire: NPSI

    Measured: Up to 3 months after inclusion

  2. Evaluate in the context of cancer the antalgic efficacy

    Questionnaire: DN4

    Measured: Up to 3 months after inclusion

  3. Evaluate in the context of cancer the antalgic efficacy

    Questionnaire: PGIC

    Measured: Up to 3 months after inclusion

  4. Evaluate in the context of cancer the tolerance profile

    The safety will be described mainly on the frequency of adverse events coded using the common toxicity criteria (NCI-CTCAE v5.0) grade. Descriptive statistics will be provided for characterizing and assessing patient's tolerance to treatment. Adverse events will be coded according to the MedDRA®.

    Measured: Up to 3 months after inclusion

  5. Evaluate in the context of cancer the quality of life including anxiety and depression

    Numeric scale (from 0 : no pain to 10: maximum pain)

    Measured: Up to 3 months after inclusion

  6. Evaluate in the context of cancer the quality of life including anxiety and depression

    Questionnaire: HADS

    Measured: Up to 3 months after inclusion

Timeline

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

  1. First posted7 Jul 2020
  2. Study start2 Feb 2021
  3. Primary completion6 Feb 2023
  4. Study completion9 Mar 2023

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
81 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04459234
Sponsor's protocol ID
ET20-130 - KETACANCER
Acronym
KETACANCER
Status last verified
Sep 2023
First submitted
1 Jul 2020
Last updated
11 Sep 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cancer and Chronic Pain, run by Centre Leon Berard at 12 sites in France.

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 11 inclusion and 3 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 11 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 12 sites in France. 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?

Describe the administration practices of the antalgic Ketamine in French CLCC (Centre de Lutte Contre le Cancer) in terms of indication (time frame: Up to 3 months after inclusion). 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 11 Sep 2023.

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KETACANCER Clinical Trial NCT04459234 | AzTrials