Intrathecal Pump Refills at Home or at the Hospital

Recruiting N/A Interventional Study
Intrathecal Pump Refill
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
82 (estimated)
Sponsor
Moens Maarten · Other
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About This Trial
The IMPROVE study is a randomized, controlled, cross-over trial designed to compare intrathecal pump refills performed at home with those carried out in the hospital. Intrathecal drug delivery (IDD) is used in patients with chronic pain or severe spasticity. Use of IDD requires the performance of pump refills about 4-6 times a year which may be a burdensome and stressful experience for patients an…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Actively receiving Intrathecal drug delivery * Stable medication dosage for at least 3 months * Dutch, French or English speaking adults Exclusion Criteria: * Life expectancy \< 6 months * Patients planned for but not yet received Intrathecal drug delivery implant * No resid…
Contacts

Maarten Moens, MD PhD

+3224775514

stimulusresearchgroup@gmail.com

CONTACT

Lisa Goudman, PhD

+32472412507

lisa.goudman@vub.be

CONTACT