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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: CTRI
Last refreshed on: 24 November 2021
Main ID:  CTRI/2014/06/004705
Date of registration: 26-06-2014
Prospective Registration: Yes
Primary sponsor: Nil
Public title: What do patients understand about methods of pain relief after surgery?
Scientific title: Patientsâ?? experience with epidural analgesia: A questionnaire survey
Date of first enrolment: 02-07-2014
Target sample size: 300
Recruitment status: Completed
URL:  http://www.ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=9237
Study type:  Observational
Study design:  Other
Method of generating randomization sequence:Not Applicable Method of allocation concealment:Not Applicable Blinding and masking:Not Applicable
 
Phase:  N/A
Countries of recruitment
India
Contacts
Name: Deepak Chavan   
Address:  Department of Anaesthesiology, Tata Memorial Hospital, Parel, Mumbai 400012 Osmanabad, MAHARASHTRA India
Telephone: 09730585988
Email: dr.deepak016@gmail.com
Affiliation:  Tata Memorial Hospital, Mumbai
Name: Deepak Chavan   
Address:  Department of Anaesthesiology, Tata Memorial Hospital, Parel, Mumbai 400012 Mumbai, MAHARASHTRA India
Telephone: 09730585988
Email: dr.deepak016@gmail.com
Affiliation:  Tata Memorial Hospital, Mumbai
Key inclusion & exclusion criteria
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:
Health Condition(s) or Problem(s) studied
Health Condition 1: null- â?¢ Adult patients undergoing epidural catheter insertion for surgical procedures. Patients with failed catheter insertions will also be included
Intervention(s)
Intervention1: Nil: Nil
Control Intervention1: Nil: Nil
Primary Outcome(s)
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

Secondary Outcome(s)
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
Secondary ID(s)
NIL
Source(s) of Monetary Support
Nil
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date: 27/03/2012
Contact:
Institutional Review Board - II
Results
Results available:
Date Posted:
Date Completed:
URL:
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