Pediatric pain control study
Not Applicable
- Conditions
- Health Condition 1: null- malignancyHealth Condition 2: C531- Malignant neoplasm of exocervix
- Registration Number
- CTRI/2016/04/006853
- Lead Sponsor
- Tata Medical Center Kolkata
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 39
Inclusion Criteria
Patients undergoing chemoport insertion- for chemotherapy for cancer treatment.
Exclusion Criteria
platelet count less than 50,000
fever
local infection
non-consenting
malignancy involving thoracic wall
known allergy to local anaesthetic drug
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain scores in the post operative periodTimepoint: Pain scores in the post operative period
- Secondary Outcome Measures
Name Time Method requirement of rescue analgesic (Fentanyl)Timepoint: 0-24 hrs in the post operative period