Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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CTRI |
Last refreshed on:
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24 November 2021 |
Main ID: |
CTRI/2014/06/004705 |
Date of registration:
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26-06-2014 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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What do patients understand about methods of pain relief after surgery?
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Scientific title:
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Patientsâ?? experience with epidural analgesia: A questionnaire survey |
Date of first enrolment:
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02-07-2014 |
Target sample size:
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300 |
Recruitment status: |
Completed |
URL:
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http://www.ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=9237 |
Study type:
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Observational |
Study design:
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Other Method of generating randomization sequence:Not Applicable Method of allocation concealment:Not Applicable Blinding and masking:Not Applicable
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Phase:
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N/A
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Countries of recruitment
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India
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Contacts
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Name:
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Deepak Chavan
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Address:
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Department of Anaesthesiology, Tata Memorial Hospital, Parel, Mumbai
400012
Osmanabad, MAHARASHTRA
India |
Telephone:
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09730585988 |
Email:
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dr.deepak016@gmail.com |
Affiliation:
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Tata Memorial Hospital, Mumbai |
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Name:
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Deepak Chavan
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Address:
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Department of Anaesthesiology, Tata Memorial Hospital, Parel, Mumbai
400012
Mumbai, MAHARASHTRA
India |
Telephone:
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09730585988 |
Email:
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dr.deepak016@gmail.com |
Affiliation:
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Tata Memorial Hospital, Mumbai |
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Key inclusion & exclusion criteria
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Inclusion criteria: Adult patients undergoing epidural catheter insertion for surgical procedures.
Patients with failed catheter insertions will also be included
Exclusion criteria: • Refusal to participate
• Epidural catheters inserted under general anaesthesia
• Patients on mechanical ventilation for more than 24 hours after surgery
Age minimum:
Age maximum:
Gender:
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Health Condition(s) or Problem(s) studied
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Health Condition 1: null- â?¢ Adult patients undergoing epidural catheter insertion for surgical procedures. Patients with failed catheter insertions will also be included
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Intervention(s)
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Intervention1: Nil: Nil Control Intervention1: Nil: Nil
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Primary Outcome(s)
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The primary outcomes will be to identify percentage of patients who have:
1. Moderate â?? severe discomfort during epidural catheter insertion
2. Poor to average pain relief with epidural analgesia
3. Complications related to use of epidural
Timepoint: 1. 24 hours after surgery
2. Day 5 or discharge, whichever is earlier
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Secondary Outcome(s)
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to identify factors (patientâ??s educational status, pre-operative knowledge, factors related to the epidural catheter insertion) associated with patient discomfort during insertion or after surgeryTimepoint: at day 5 after surgery
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Source(s) of Monetary Support
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Nil
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Ethics review
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Status: Approved
Approval date: 27/03/2012
Contact:
Institutional Review Board - II
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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