- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03236714
Awareness and Compliance Among Health Professionals of the Preoperative Fasting Period
July 28, 2017 updated by: Hakan Tapar, Tokat Gaziosmanpasa University
Awareness and Compliance Among Health Professionals of the Preoperative
Preoperative fasting is mandatory for anesthetic induction.
This period of fasting is probably greater due to delays in the surgical theater and changes in daily operation schedules.Investigators want to resarch between the prescribed and the actual preoperative fasting time.
Study Overview
Status
Unknown
Conditions
Detailed Description
Before surgery, the patients will be asked to liquid, solid fasting times.and
whether information is given about the fasting period.In addition, the appropriateness of health personnel to new guidelines for preoperative fasting will be evaluated.At the end of the study, the desired duration of fasting, clinical practice and trends of health personnel will be investigated.
Study Type
Observational
Enrollment (Anticipated)
300
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Tokat, Turkey, 60200
- Recruiting
- Hakan Tapar
-
Contact:
- Hakan Tapar, Assist .Prof
- Phone Number: 3496 03562129500
- Email: hakantapar@hotmail.com
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 day to 80 years (ADULT, OLDER_ADULT, CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients planning elective surgery according to the study
Description
Inclusion Criteria:
- Between 1 day and 80 years
- Elective surgery
- Oral fed
- American Society of Anesthesiologists score of 1 or 3
Exclusion Criteria:
- Intensive care patient
- Parenteral nutrition
- Emergency surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The patients' preoperative fasting period
Time Frame: one time in two months
|
Determination of fasting period before surgery trends of new guidelines for preoperative fasting.
|
one time in two months
|
|
Training of health workers
Time Frame: one time in two months
|
Determining health personnel's application
|
one time in two months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
July 24, 2017
Primary Completion (ANTICIPATED)
September 1, 2017
Study Completion (ANTICIPATED)
September 5, 2017
Study Registration Dates
First Submitted
July 24, 2017
First Submitted That Met QC Criteria
July 28, 2017
First Posted (ACTUAL)
August 2, 2017
Study Record Updates
Last Update Posted (ACTUAL)
August 2, 2017
Last Update Submitted That Met QC Criteria
July 28, 2017
Last Verified
July 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 17-KAEK-005
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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