A SAD Study to Evaluate the Safety, Tolerability and PK/PD of iN1011-N17 in Healthy Volunteers
NCT05496205
Arthritis, Chronic Pain
Melbourne, Victoria, Australia
View Trial DetailsNCT Number: NCT00627289
Chronic postherniotomy pain affects every day activities in 5-8% of patients. However, no established treatment for this pain syndrome exists and previous reports on the effect of surgical intervention suffer from methodological problems. The neurophysiological characteristics suggest that pain arises from deeper neuronal structures injured during surgery or by ongoing inflammation from the mesh. This study investigates the effect of removing inserted mesh and compressed nerves on pain related daily impairment of activities assessed by the validated AAS questionnaire before and 6 months after surgery
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Notify Me18 year and older
All sexes
Observational
Rigshospitalet, Copenhagen, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 6 months
Time frame: 6 months
Rigshospitalet, Denmark
Other
The Effect of Selective Neurectomy and Mesh Removal on Chronic Postherniotomy Pain
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