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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. |
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Register:
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CTRI |
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Last refreshed on:
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19 December 2023 |
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Main ID: |
CTRI/2014/12/005243 |
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Date of registration:
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03-12-2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Relevance of routinely prescribed laboratory tests before minor and intermediate grade of elective surgery
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Scientific title:
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Relevance of routinely prescribed preoperative investigations for patients undergoing minor and intermediate elective surgery - RRPPI |
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Date of first enrolment:
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01-03-2010 |
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Target sample size:
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200 |
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Recruitment status: |
Completed |
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URL:
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http://www.ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=9454 |
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Study type:
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Observational |
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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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Jyotirmay Kirtania
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Address:
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9/1/2 B C Roy Path, Shyamnagar, North 24 Parganas
743127
North Twentyfour Parganas, WEST BENGAL
India |
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Telephone:
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9330960138 |
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Email:
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jyoti.kirtania@rediffmail.com |
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Affiliation:
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Institute of Postgraduate Medical Education and Research |
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Name:
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Partha Sarathi Dutta
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Address:
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Department of Surgery, Ronald Ross Building, SSKM Hospital, 244 A J C Bose Road
743127
Kolkata, WEST BENGAL
India |
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Telephone:
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9330960138 |
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Email:
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jyoti.kirtania@rediffmail.com |
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Affiliation:
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Institute of Postgraduate Medical Education and Research |
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Key inclusion & exclusion criteria
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Inclusion criteria: Patients between 18 and 60 years of age with mild or no comorbid medical illness undergoing minor and intermediate grade elective surgery were included.
Exclusion criteria: • Unwilling patients
• Patients with malignancy
• Patients with severe comorbidity (severe respiratory, cardiovascular, neurological and renal disease)
• Pregnancy
Age minimum:
Age maximum:
Gender:
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Health Condition(s) or Problem(s) studied
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Primary Outcome(s)
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The overall outcome after surgery, defined as the
occurrence of any perioperative complication i.e. surgical, anesthetic or medical morbidity and mortality during or within 30 days of surgery.Timepoint: The overall outcome after surgery, defined as the
occurrence of any perioperative complication i.e. surgical, anesthetic or medical morbidity and mortality during or within 30 days of surgery.
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Secondary Outcome(s)
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Co-relation of preoperative clinical history questionnaire, standardized physical examination, and predefined set of routine laboratory investigations with the outcome of surgeryTimepoint: Within 30 days of surgery, including the day of surgery.
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Source(s) of Monetary Support
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Funded by the principal investigator, Dr Partha Sarathi Dutta
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Ethics review
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Status: Approved
Approval date: 04/01/2010
Contact:
Institutional Ethics Committee, Institute of POst Graduate Medical Education and Research, Kolkata
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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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