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.
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
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.
- Conditions
- Cancer, Chronic Pain, Neuropathic Pain, Opioid Use
- 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):
- 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
- Administration protocol: route, posology, duration, administration sequence, premedication
- Antalgic efficacy
- Tolerance profile
- Quality of life, anxiety and depression evaluations
What is being measured
The primary outcome is the main question the study is designed to answer.
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
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)
Evaluate in the context of cancer the antalgic efficacy
Questionnaire: NPSI
Measured: Up to 3 months after inclusion
Evaluate in the context of cancer the antalgic efficacy
Questionnaire: DN4
Measured: Up to 3 months after inclusion
Evaluate in the context of cancer the antalgic efficacy
Questionnaire: PGIC
Measured: Up to 3 months after inclusion
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
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
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.
- First posted7 Jul 2020
- Study start2 Feb 2021
- Primary completion6 Feb 2023
- Study completion9 Mar 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for CancerStudies of the same condition, open and under way.
- More trials run by Centre Leon BerardThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Centre Leon Berard
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Gisèle CHVETZOFF, MD, Principal investigator, Centre Leon Berard
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
Study at a glance
From the registry record, last updated by the sponsor on 11 Sep 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- KETACANCER: Prospective Multicentre Study of the Use of Ketamine in the Treatment of Refractory Chronic Pain in the French CLCC
- ClinicalTrials.gov ID
- NCT04459234
- Acronym / sponsor ID
- KETACANCER / ET20-130 - KETACANCER
- Conditions
- Cancer, Chronic Pain, Neuropathic Pain, Opioid Use
- Keywords
- Cancer, Palliative care, Ketamine, Chronic pain
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 81 participants (actual)
- Lead sponsor
- Centre Leon BerardUniversity, hospital or other
- Study start
- 2 Feb 2021 (actual)
- Primary completion
- 6 Feb 2023 (actual)
- Study completion
- 9 Mar 2023 (actual)
- First posted
- 7 Jul 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (11 listed)
- 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:
Key exclusion criteria (3 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Ketamine use in CLCC sites (indication and administration protocol)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 | Drug | – |
Primary outcome
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
neuropathic sequelae pains, morphine additional effect or morphine withdrawal, intensity, localisation
Describe the administration practices of the antalgic Ketamine in French CLCC (Centre de Lutte Contre le Cancer) in terms of administration protocol
Time frame: Up to 3 months after inclusion
route, posology, duration, administration sequence, premedication
6 secondary outcomes
Evaluate in the context of cancer the antalgic efficacy
Time frame: Up to 3 months after inclusion
Evaluate in the context of cancer the antalgic efficacy
Time frame: Up to 3 months after inclusion
Evaluate in the context of cancer the antalgic efficacy
Time frame: Up to 3 months after inclusion
Evaluate in the context of cancer the tolerance profile
Time frame: Up to 3 months after inclusion
Evaluate in the context of cancer the quality of life including anxiety and depression
Time frame: Up to 3 months after inclusion
Evaluate in the context of cancer the quality of life including anxiety and depression
Time frame: Up to 3 months after inclusion
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Sep 2023.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Gisèle CHVETZOFF, MD principal investigator
Centre Leon Berard
12 sites in 1 country: see every site and its status.
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.