Health Condition 1: C408- Malignant neoplasm of overlappingsites of bone and articular cartilage of limb
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Tata Memorial Hospital
Not Any
Eligibility
Inclusion criteria
Inclusion criteria: 1.age group 13-65 years 2.gender: both male and female 3.patients undergoing curative surgery for histologically confirmed bone and soft tissue tumors of the extremities and pelvis with or without adjuvant chemotherapy.
Exclusion criteria
Exclusion criteria: 1. Patients with active symptoms of neuropathic pain or Chemotherapy-induced Peripheral Neuropathy (CIPN) at the time of surgery. 2. Refusal to consent 3. Patients with inability to comprehend or understand the questionnaire
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study the incidence of neuropathic pain in patients undergoing BST surgery using NP painDETECT questionnaire 72 hours post-surgery.Timepoint: To study the incidence of neuropathic pain in patients undergoing BST surgery using NP painDETECT questionnaire 72 hours post-surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| To understand incidence of symptoms similar to but not mounting to neuropathic pain in the post-operative period (painDETECT score 13-18 â??possibleâ?? NP).Timepoint: after 3 month followup;To understand prevalent pain scores and satisfaction to pain management in the study population (to be captured on NRS 0-10).Timepoint: after 3 month followup;To understand the predisposing factors for neuropathic painTimepoint: at the end of study enrollment | — |
Countries
India
Contacts
Public ContactDrSakshi Sharma
Tata Memorial Hospital
Outcome results
None listed