Use of Ketamine in Severe Pain Syndromes
Use of Intravenous Ketamine in Patients with Severe Chronic Pain Syndromes
1 other identifier
observational
89
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 1, 2024
CompletedStudy Start
First participant enrolled
August 1, 2024
CompletedFirst Posted
Study publicly available on registry
August 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 20, 2025
CompletedFebruary 25, 2025
August 1, 2024
7 months
August 1, 2024
February 24, 2025
Conditions
Outcome Measures
Primary Outcomes (3)
Patient satisfaction
A scale (good-medium-no effect) of the efficacity of ketamine on their pain syndrome
6 month
DN4
Neuropathic pain scale 4
6 month
VAS
Visual analog scale of the pain intensity
6 month
Secondary Outcomes (1)
Concomitant pain medications
6 month
Eligibility Criteria
All patients who received ketamine as treatment for a pain syndrome during january 2010 until june 2024 at Erasme University Hospital
You may qualify if:
- \- All patients who received ketamine as treatment for a pain syndrome during january 2010 until june 2024 at Erasme University Hospital
You may not qualify if:
- Age \< 18 years
- Patients who expressed their opposition to the use of their medical data
- incomplete medical chart
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hôpital Universitaire de Bruxelles - Hôpital erasme
Brussels, 1070, Belgium
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 1, 2024
First Posted
August 5, 2024
Study Start
August 1, 2024
Primary Completion
February 20, 2025
Study Completion
February 20, 2025
Last Updated
February 25, 2025
Record last verified: 2024-08