The goal of this prospective observational study is to observe the effectiveness of pain management interventions in patients with abdominal and pelvic cancer pain. The main question\[s\] it aims to answer are: * The effectiveness of pain management interventions. * The frequency of pain intervention procedures and side effects and complications of pain management interventions
Study Type
OBSERVATIONAL
Enrollment
100
Patient reported NRS score
Numeric Rating Score from 0 (no pain)- 10 (severe pain)
Time frame: First visit and then at 3 months
Number of patients
Number of patients on whom the intervention is performed.
Time frame: From 2 weeks to 3 months.
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