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OBSERVATIONAL STUDY OF THE MANAGEMENT OF PATIENTS WITH CHRONIC PAIN

OBSERVATIONAL STUDY OF THE MANAGEMENT OF PATIENTS WITH CHRONIC PAIN

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03319238
Acronym
OKAPI
Enrollment
1000
Registered
2017-10-24
Start date
2016-07-07
Completion date
2018-11-01
Last updated
2017-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain

Keywords

Chronic pain, Neuropathic pain, Ketamine, Concomitant treatment, Adverse effect

Brief summary

The aim of this study is to evaluate the safety of use, benefits and risks of repeated use of ketamine for each patient with chronic pain in different structures of pain management.

Detailed description

This is an observational, longitudinal and multicenter study about use of ketamine. Benefits are assessed with pain intensity, anxiety, depression, quality of life and global impression of change. Risks are also assessed with adverse event collection.

Interventions

OTHERketamine

The aim of this study is to evaluate the safety of use, benefits and risks of repeated use of ketamine for each patient with chronic pain in different structures of pain management.

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged over 18 years * Patients with chronic pain (more than 6 months) * Patients with peripheral or central neuropathic pain, fibromyalgia, algoneurodystrophy

Exclusion criteria

* Patient under 18 years of age, * Patient not requiring prescription of ketamine

Design outcomes

Primary

MeasureTime frameDescription
Descriptive analysis of benefitAt baselineBenefits (pain release after ketamine use) will be assessed by the Pain by the Numerical Pain Rating Scale (NPRS): the scale ranges from 0 no pain to 10 maximal tolerable pain, and risks will be assessed by collecting the ketamine adverse events reported by the patient and by the physician.

Secondary

MeasureTime frameDescription
Descriptive analysis of risk (by collecting adverse event) of ketamine use.At baselineBiological statements will be collected during the usual care of patients, if possible (ASAT, ALAT, total bilirubin, conjugate bilirubin, free bilirubin, gamma glutamyl transferase, alkaline phosphatase,…)
Neuropathic Pain in 4 questions (DN4),At baselineThe Neuropathic pain in 4 questions (DN4) at baseline only. DN4 is a clinical tool for the diagnosis of neuropathic pain. This questionnaire has four questions divided into 10 items related to the interview (ie, symptoms) and to the sensory examination (ie, signs). The investigator asks and examines the patient and notes a response no or yes for each item: yes is scored as 1 and no is scored as 0. The sum of scores gives the total score of the patient (/10). DN4 is considered as positive if the patient obtains a score of 4/10.
Patient Global Impression of Change, the characteristics of pain (PGIC)At baselineThe Patient Global Impression of Change is a scale of global perception of change (Deterioration or Improvement) realized at each telephone call except for baseline. This scale is graduated from 1 = very strongly improved to 7 = very strongly aggravated
Emotional status by Hospital Anxiety and Depression scale (HAD)At baselineThe HAD scale is a self-administered questionnaire in 14 items completed by the patient. It is used to determine the levels of anxiety and depression. Seven of the items relate to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 and 21 for either anxiety or depression. Global score ranges from 0 to 42.
Quality of life (Short Form 12 items Short Form survey)At baselineassessed by a quality of life questionnaire (Short Form 12 items Short Form survey (SF12)

Countries

France

Contacts

Primary ContactPatrick LACARIN
placarin@chu-clermontferrand.fr04 73 75 11 95

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026