Enrolling by InvitationN/Aketamine

Long-term Pain Modulation by Intravenous Esketamine in CRPS

Sponsored by Erasmus Medical Center

NCT ID
NCT05212571
Target Enrollment
60 participants
Start Date
2022-04-19
Est. Completion
2027-10-01

About This Study

Intravenous administration of esketamine is an effective recognized therapeutic option in refractory pain in CRPS, which sometimes in at least a part of the patients has a prolonged therapeutic effect. Unfortunately, CRPS literature contains a wide range of ketamine dosing regimens with the result that clinical protocols on dosage and administration are very heterogeneous. The current esketamine regimen in Erasmus MC consists of a 6-day hospital admission for continuous administration. In the Netherlands, both inpatient and outpatient esketamine treatments are offered. Inpatient and outpatient ketamine treatments have never been compared in randomized controlled trials and it is therefore unknown whether these two dosing regimens are equally effective. The primary objective is to demonstrate non-inferiority of experimental esketamine administration of 6x 1 day per 2 weeks (in total 3 months) as compared with standard esketamine administration of 1x 6 consecutive days. The end of study is at 6 months after the start of the study/treatment.

Conditions Studied

Complex Regional Pain SyndromesCRPS (Complex Regional Pain Syndromes)

Interventions

  • S-ketamine infusion inpatient setting
  • S-ketamine infusion outpatient setting

Eligibility

Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Meeting the new International Association for the Study of Pain (IASP) diagnostic criteria for CRPS ("the Budapest Criteria) (Harden et al., 2010) or having met the new IASP diagnostic criteria of CRPS ("CRPS with Remission of Some features") (Goebel et al., 2021).
* Willing and capable to participate in the study.
* CRPS in one upper extremity and/or CRPS in one lower extremity
* Treatment in an elective setting.
* Adequate comprehension of the Dutch language
* Age ≥ 18 years

Exclusion Criteria:

* Severe liver disease
* Psychiatric (schizophrenia, psychosis, delirium, manic depression)
* Active substance abuse
* Intoxication with alcohol or other substances
* Poorly controlled hypertension
* Unstable angina
* High-risk coronary vascular disease
* Heart failure
* Elevated intracranial pressure
* Elevated intraocular pressure
* Thyrotoxicosis
* Pregnancy
* Combination with derivates of xanthines (theophylline) or ergometrine

Study Locations (1)

Erasmus MC
Rotterdam, South Holland, Netherlands

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source