NCT03236714

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2017

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 24, 2017

Completed
Same day until next milestone

Study Start

First participant enrolled

July 24, 2017

Completed
9 days until next milestone

First Posted

Study publicly available on registry

August 2, 2017

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2017

Completed
4 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 5, 2017

Completed
Last Updated

August 2, 2017

Status Verified

July 1, 2017

Enrollment Period

1 month

First QC Date

July 24, 2017

Last Update Submit

July 28, 2017

Conditions

Preoperative Fasting

Outcome Measures

Primary Outcomes (2)

  • The patients' preoperative fasting period

    Determination of fasting period before surgery trends of new guidelines for preoperative fasting.

    one time in two months

  • Training of health workers

    Determining health personnel's application

    one time in two months

Eligibility Criteria

Age1 Day - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients planning elective surgery according to the study

You may qualify if:

  • Between 1 day and 80 years
  • Elective surgery
  • Oral fed
  • American Society of Anesthesiologists score of 1 or 3

You may not qualify if:

  • Intensive care patient
  • Parenteral nutrition
  • Emergency surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Hakan Tapar

Tokat Province, 60200, Turkey (Türkiye)

RECRUITING

Hakan Tapar

Tokat Province, 60200, Turkey (Türkiye)

RECRUITING

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assist.Prof

Study Record Dates

First Submitted

July 24, 2017

First Posted

August 2, 2017

Study Start

July 24, 2017

Primary Completion

September 1, 2017

Study Completion

September 5, 2017

Last Updated

August 2, 2017

Record last verified: 2017-07

Data Sharing

IPD Sharing
Will not share

Locations

TU(2)