Quantitative Sensory Testing and Conditioned Pain Modulation in patients after cervical percutaneous cordotomy - QST and CPM after cordotomy

Erasmus MC, Universitair Medisch Centrum Rotterdam0 sites10 target enrollmentTBD

Conditionstherapieresistente, oncologische pijn cancer pain 10027655

Overview

Phase: N/A
Intervention: Not specified
Conditions: therapieresistente, oncologische pijn
Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam
Enrollment: 10
Status: Not Yet Recruiting
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

2 years ago

Study Type

Observational non invasive

Investigators

Sponsor

Erasmus MC, Universitair Medisch Centrum Rotterdam

Eligibility Criteria

Inclusion Criteria

•\-Cervical percutaneous cordotomy, 2\-4 weeks prior to the sensory testing
•\-The cervical percutaneous cordotomy must have been successfull: a loss of vital sensibility (determined by a positive pin\-prick: a sharp pinch applied with a paper clip) caudal to dermatome C5, contralateral to the cordotomy side.
•\-Informed consent must have been obtained

Exclusion Criteria

•\-Neurological disease/ nerve conduction disorder, which will influence the results of a bilateral QST measurement
•\-Inability to understand and speak in dutch
•\-When the sensory testing will be too much of a burden for the patient (in terms of psychological capacity, logistic problems, or a very limited prognosis). The attending Anesthesiologist/Pain Specialist (P. Zomers) will determine this.

Outcomes

Primary Outcomes

Not specified

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