Effectiveness of Pain Management Interventions in Patients With Abdominal and Pelvic Cancer
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Abdominal Cancer. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Effectiveness of Pain Management Interventions in Patients With Abdominal and Pelvic Cancer in a Tertiary Care Hospital: A Prospective Observational Study
Overview
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
Primary outcome measures
- Patient reported NRS score [Time frame: First visit and then at 3 months]
Secondary outcome measures (1)
- Number of patients [Time frame: From 2 weeks to 3 months.]
Eligibility criteria
Inclusion criteria
- Patients with chronic pain due to abdominal and pelvic cancer
- Both Male and Female
- Ages18-65 years
- Patients who with recurrence or metastasis
Exclusion criteria
- Patients who refuse to give consent
- Patients who were lost to follow up after initial visit or assessment
- History of severe depression or psychiatric illness
- History of surgical procedure due to cancer
- Patients with DNR code
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07357350 · 2025-12177-38695