Preoperative FastingNCT03236714
Awareness and Compliance Among Health Professionals of the Preoperative Fasting Period
An observational study of Preoperative Fasting, run by Tokat Gaziosmanpasa University at 2 sites in Turkey (Türkiye).
Trial summary
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. Read more about this study
- Who is it for?
- Ages 1 day to 80 yearsHealthy volunteers can take part
- Conditions the study is for
- Preoperative Fasting
- How many people
- 300 participants
- Where
- 2 sitesTurkey (Türkiye)
- Study dates
- 24 Jul 2017to 5 Sep 2017
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 1 day to 80 years
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: Patients planning elective surgery according to the study
Who may be able to join
- Between 1 day and 80 years
- Elective surgery
- Oral fed
- American Society of Anesthesiologists score of 1 or 3
Who cannot join
- Intensive care patient
- Parenteral nutrition
- Emergency surgery
Trial locations and contacts
2 sites in 1 country.
Turkey (Türkiye)2 sites, 2 recruiting
- Recruiting
Hakan Tapar
Tokat Province, 60200
Hakan Tapar, Assist.Prof, 03562129500 ext. 3496, hakantapar@hotmail.com
- Recruiting
Hakan Tapar
Tokat Province, 60200
Hakan Tapar, Assist .Prof, 03562129500 ext. 3496, hakantapar@hotmail.com
About this study
Official title: 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.
Read the 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.
- Conditions
- Preoperative Fasting
What is being measured
The primary outcome is the main question the study is designed to answer.
The patients' preoperative fasting period
Determination of fasting period before surgery trends of new guidelines for preoperative fasting.
Measured: one time in two months
Training of health workers
Determining health personnel's application
Measured: one time in two months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Aug 2017
- Study start24 Jul 2017
- Primary completion1 Sep 2017 (estimated)
- Study completion5 Sep 2017 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Preoperative FastingStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 300 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Tokat Gaziosmanpasa University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Hakan Tapar, Tokat Gaziosmanpasa University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03236714
- Sponsor's protocol ID
- 17-KAEK-005
- Status last verified
- Jul 2017
- First submitted
- 24 Jul 2017
- Last updated
- 2 Aug 2017
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Aug 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Awareness and Compliance Among Health Professionals of the Preoperative
- ClinicalTrials.gov ID
- NCT03236714
- Acronym / sponsor ID
- 17-KAEK-005
- Conditions
- Preoperative Fasting
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- Tokat Gaziosmanpasa UniversityUniversity, hospital or other
- Study start
- 24 Jul 2017 (actual)
- Primary completion
- 1 Sep 2017 (estimated)
- Study completion
- 5 Sep 2017 (estimated)
- First posted
- 2 Aug 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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 design
- Observational model
- Other
- Time perspective
- Prospective
Who may qualify
- Ages
- 1 day to 80 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients planning elective surgery according to the study
Key inclusion criteria (4 listed)
- Between 1 day and 80 years
- Elective surgery
- Oral fed
- American Society of Anesthesiologists score of 1 or 3
Key exclusion criteria (3 listed)
- Intensive care patient
- Parenteral nutrition
- Emergency surgery
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
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.
Training of health workers
Time frame: one time in two months
Determining health personnel's application
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Aug 2017.
- Individual participant dataSharing planned: No
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Intermittent Fasting Versus Carbohydrate Drinks Before Surgery
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Comparative Effectiveness
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Preoperative Fasting and Perioperative Outcomes in Children Undergoing Elective Circumcision
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Gastric Emptying After a Yoghurt Breakfast in Children: a Pilot Study
Preoperative Fasting
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Preoperative Fasting, run by Tokat Gaziosmanpasa University at 2 sites in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 2 Aug 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The patients' preoperative fasting period (time frame: one time in two months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Aug 2017.