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Study to assess the need and type of pain killers analgesics prescribed at discharge for patients undergoing cancer surgery.

Not yet recruiting
Conditions
Neoplasms,
Registration Number
CTRI/2025/03/082549
Lead Sponsor
Department of Anesthesia Critical Care and Pain
Brief Summary

After taking approval from Institutional ethics committee, 30 patients from each DMG (Thoracic, Gastrointestinal, Gynecology, Urology, Bone and soft tissue, Breast, and Head neck surgeries), and a total of 210 consecutive patients who are discharged within 96 hours of major surgery will be enrolled in the study after taking valid informed consent.

Based on the feedback from surgeons, patients planned for discharge within 96 hours will be consented. After consent, patient will be given hard copy of BPI and the scale will be explained to them.  The analgesics on discharge card will be noted. If the patients are asked to follow-up with in a week, then at first follow up or else telephonically, the pain assessment based on BPI will be done. In case patient has severe pain not being controlled by analgesic advised then a follow-up with the unit and if needed pain clinic will be advised.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
210
Inclusion Criteria

All adult patients upto 80 years following major oncology surgery with discharge within 96 hours of surgery will be included.

Exclusion Criteria
  • Refusal to participation.
  • 2.Emergenecy surgeries.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total number of patients in moderate -severe pain a week after discharge from the hospital following major onco surgeries, assessed by analysing the severity of average pain recorded in the short form of Brief Pain Inventory ( BPI)a week after discharge from the hospital
Secondary Outcome Measures
NameTimeMethod
1.Number of patients (in percentage) advised round the clock analgesics at discharge, since evaluation will be done at end of a week – this assessment will be recorded for the first 2 days2.The pattern of analgesic prescribed as number of analgesics from different sub types- opioid, PCM, NSAIDS, adjutants
5.Number of patients who did not take medications as advised6.Number of patients who needed additional analgesics than prescribed in first week of surgery. The source of additional analgesics will also be noted as local doctor/ local dispensary /medications left over from previous prescriptions.

Trial Locations

Locations (1)

Tata Memorial Hospital

🇮🇳

Mumbai, MAHARASHTRA, India

Tata Memorial Hospital
🇮🇳Mumbai, MAHARASHTRA, India
Dr Sumitra G Bakshi
Principal investigator
02224177058
sumitrabakshi@yahoo.in

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