Oncology Pain Clinical Trial
— PGSOfficial title:
Pituitary Gland Stimulation for Cancer Pain Relief
Patients will undergo an implantation of an extradural pituitary surface electrode in the pituitary fossa. The electrode will be attached to a neurostimulator via which the patient will receive up to 8 (patient requested) stimulations per day.
Status | Recruiting |
Enrollment | 10 |
Est. completion date | January 1, 2024 |
Est. primary completion date | January 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Adult patient - In palliative phase of metastatic disease, without options for further systemic treatment or radiotherapy - Inadequately controlled pain with standard care - Most prominent part of experienced pain is nociceptive - Karnofsky Performance Score =30 Exclusion Criteria: - Not fit for general anesthesia - Pregnancy - Unfavorable local anatomy for PGS, due to a disease process, or anatomical configuration - Clinical signs of posterior pituitary gland disfunction - Recent history of alcohol or drug abuse - Severe immunodeficiency - Need for anticoagulation therapy that cannot be abrogated for surgery - Need for subsequent MRI-imaging - Cognitive impairments prohibiting full understanding of study and ability to provide informed consent - Not able to adequately communicate in Dutch or English |
Country | Name | City | State |
---|---|---|---|
Netherlands | Leiden University Medical Center | Leiden |
Lead Sponsor | Collaborator |
---|---|
Leiden University Medical Center |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Perceived pain | Numeric Rating Scale (0= no pain, 10=most severe pain) | 4 months | |
Primary | Pain Medication | Morphine Equivalent Doses for background and escape medication | 4 months |
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---|---|---|---|
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