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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05230238
Other study ID # P21.036
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 12, 2021
Est. completion date January 1, 2024

Study information

Verified date March 2023
Source Leiden University Medical Center
Contact Wouter van Furth, MD, Phd
Phone +31715162109
Email w.r.van_furth@lumc.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Pituitary gland stimulation
Pituitary gland stimulation via an surface electrode connected to an external neurostimulator

Locations

Country Name City State
Netherlands Leiden University Medical Center Leiden

Sponsors (1)

Lead Sponsor Collaborator
Leiden University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

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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