- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06537375
Use of Ketamine in Severe Pain Syndromes
February 24, 2025 updated by: Erasme University Hospital
Use of Intravenous Ketamine in Patients with Severe Chronic Pain Syndromes
Ketamine has been shown to have a certain efficiency in chronic pain syndromes.
However, it is still not clearly known what is its efficiency and how ketamine is used in real world patients.
In this retrospective study, all patients treated with ketamine for chronic pain in our hospital will be reviewed.
Patients demographics, pain syndromes as well as outcome criteria will be collected to describe the use of ketamine in pain syndromes.
Study Overview
Status
Completed
Detailed Description
The American Society of Regional Anesthesia and Pain Medicine, together with the American Academy of Pain and the American Society of Anesthesiologists published a consensus guideline in 2018 on the use of ketamine in chronic pain.
A review of medical charts of all patients who received ketamine for chronic pain between january 2010 and june 2024 will be done.
Demographic data, detailed pain scores, as well as description of the type of pain will be collected.
Ketamine usage will be recorded for the dosage, as well as duration of the treatment.
Outcome will be measured by before/after pain scores for neuropathic pain, as well as on a visual analog scale.
A more global score (good-medium-no effect) will also be collected to get the patient's impression on their treatment.
Concomitant pain medication will be collected.
Study Type
Observational
Enrollment (Actual)
89
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Brussels, Belgium, 1070
- Hopital Universitaire de Bruxelles - Hopital Erasme
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
All patients who received ketamine as treatment for a pain syndrome during january 2010 until june 2024 at Erasme University Hospital
Description
Inclusion Criteria:
- All patients who received ketamine as treatment for a pain syndrome during january 2010 until june 2024 at Erasme University Hospital
Exclusion Criteria:
- Age < 18 years
- Patients who expressed their opposition to the use of their medical data
- incomplete medical chart
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient satisfaction
Time Frame: 6 month
|
A scale (good-medium-no effect) of the efficacity of ketamine on their pain syndrome
|
6 month
|
|
DN4
Time Frame: 6 month
|
Neuropathic pain scale 4
|
6 month
|
|
VAS
Time Frame: 6 month
|
Visual analog scale of the pain intensity
|
6 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Concomitant pain medications
Time Frame: 6 month
|
Number of concomitant pain medications used by the patient
|
6 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2024
Primary Completion (Actual)
February 20, 2025
Study Completion (Actual)
February 20, 2025
Study Registration Dates
First Submitted
August 1, 2024
First Submitted That Met QC Criteria
August 1, 2024
First Posted (Actual)
August 5, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 24, 2025
Last Verified
August 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SRB2024171
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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