comparison of intervention with pain medication in the management of pain and improvement of quality of life in upper abdominal malignancy.
Phase 2
- Conditions
- Health Condition 1: null- Upper abdominal cancer patient with moderate tosevere pain presenting to pain clinic.
- Registration Number
- CTRI/2018/06/014528
- Lead Sponsor
- AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
•Age more than 18 years
•Either gender
•Patients have agreed to participate in the study and have signed written informed consent.
•Admitted in palliative care ward or attending Palliative care OPD at IRCH
•NRS >4 (Moderate to severe pain)
•Somatic, visceral or mixed pain
Exclusion Criteria
•Psychiatric disorder
•Patients refusal to give consent to participate in the study
•Patients with delirium or obtundation
•Deranged coagulation profile
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method