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Trial registered on ANZCTR
Registration number
ACTRN12618000056291
Ethics application status
Approved
Date submitted
26/08/2017
Date registered
17/01/2018
Date last updated
17/01/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Quality of obstetric care by the type of anaesthesia for caesarean section
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Scientific title
Quality of obstetric care by the type of anaesthesia for caesarean section at a tertiary care hospital: a retrospective analysis
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Secondary ID [1]
292701
0
None
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Universal Trial Number (UTN)
U1111-1201-0854
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
cesarean section
304457
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Condition category
Condition code
Anaesthesiology
303793
303793
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0
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Other anaesthesiology
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Reproductive Health and Childbirth
303794
303794
0
0
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Childbirth and postnatal care
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Study involves all patients undergoing caesarean section under general, spinal or epidural anaesthesia. All of the patients are managed by standard, routine anaesthesia methods and monitored by standard methods. Standard monitored data will be recorded for all patients: age, weight, height, BMI, parity, gestational weeks, indication for C-section, urgency category of C-section, type and dose of drugs used and experience level of staff involved. For cases of conversion of regional to general anaesthesia additional variables observed are time between regional anaesthesia applications and general anaesthesia, as well as number of top-ups. Participants are observed until discharge from the ICU or PACU.
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Intervention code [1]
298942
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Not applicable
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Comparator / control treatment
Only one group of patients was included in the study.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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The composite primary outcome is the rate of general anesthesia, rate of regional anesthesia and rate of conversions from regional to general anaesthesia for caesarean section which are all together considered (by the reccommendations of RCOG) as being parameters of the quality of obstetric care. The mentioned outcome will be assesed by the review of medical records.
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Assessment method [1]
303157
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Timepoint [1]
303157
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C-section incision time
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Secondary outcome [1]
338056
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Variable difference between C-sections in successful and failed epidural anaesthesia is assesed by the medical record, i.e. if in the same patient, both epidural and general anesthesia were used, then is obvious to conclude that these are the cases of failed epidural anesthesia (because there was a necessity to induce general anesthesia, despite the fact that epidural anesthesia was already applied in the particular patient).
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Assessment method [1]
338056
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Timepoint [1]
338056
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C-section incision time
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Eligibility
Key inclusion criteria
Patients who underwent C-section
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Incomplete data for type of anaesthesia used.
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Retrospective
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Statistical methods / analysis
Participants are all women who underwent C-section in our clinic in a three-year period. Statistical analysis will be done on a Mac computer using SPSS software version 23. For differences in demographical variables between patients undergoing C-section in general, regional or conversions of regional to general anaesthesia a One-way ANOVA test will be used. For differences in demographical variables between patients who underwent successful or failed epidural anaesthesia t-test will be used. For comparison of nominal variables (experience level of staff, urgency categories) Chi square test will be used. In all tests, p<0.05 will be considered significant.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
25/08/2017
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Date of last participant enrolment
Anticipated
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Actual
1/11/2017
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Date of last data collection
Anticipated
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Actual
1/11/2017
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Sample size
Target
3000
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Accrual to date
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Final
3082
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Recruitment outside Australia
Country [1]
9156
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Croatia
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State/province [1]
9156
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Funding & Sponsors
Funding source category [1]
297341
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Hospital
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Name [1]
297341
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Department for Anaesthesiology and Intensive Care Medicine, Clinic for Surgery, Clinical Hospital Center Zagreb, Zagreb, Croatia
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Address [1]
297341
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Kispaticeva 12, 10000 Zagreb, Croatia
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Country [1]
297341
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Croatia
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Primary sponsor type
Hospital
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Name
Department for Anaesthesiology and Intensive Care Medicine, Clinic for Surgery, Clinical Hospital Center Zagreb, Zagreb, Croatia
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Address
Kispaticeva 12, 10000 Zagreb, Croatia
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Country
Croatia
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Secondary sponsor category [1]
296318
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None
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Name [1]
296318
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Address [1]
296318
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Country [1]
296318
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
298441
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Ethical Committe of the Obstetrics and Gynecology Clinic
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Ethics committee address [1]
298441
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Petrova 13 10000 Zagreb
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Ethics committee country [1]
298441
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Croatia
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Date submitted for ethics approval [1]
298441
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21/08/2017
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Approval date [1]
298441
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24/08/2017
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Ethics approval number [1]
298441
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021-1/121-17
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Summary
Brief summary
Royal College of Anaesthetists (RCOG), in their Audit from 2012, suggests that an indicator of the quality of obstetric care, except the rate of general and regional anaesthesia, should be the rate of conversion of regional analgesia to general anaesthesia for caesarean section. That rate, depending on the urgency category of C-section, should not be larger than 1% for category 4 and 15% for category 1. The primary goal of this study is to compare types of anaesthesia used at our department with RCOG standards by retrospectively analysing the type of anaesthesia used for C-section during the three-year period. The secondary goal is to establish which factors led to failure of regional anaesthesia for C-section.
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Trial website
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Trial related presentations / publications
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Public notes
Ethics approval was attained after recruitment of the first participant because at the time of the recruitment of the first participant, there was still no initiative to conduct this particular trial. However, the above mentioned Ethical Committe agreed to approve this research, because all of the recruited patients have read and signed the informed consent in which they agreed that all of the data in their medical records can be used for scientific purpose, whether in ongoing trials or in any future retrospective trials. In the informed consent (which was signed by all of the recruited patients) it was also stated that the personal data of each particular patient is secured.
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Attachments [1]
1989
1989
0
0
/AnzctrAttachments/373511-consent form.docx
(Participant information/consent)
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Contacts
Principal investigator
Name
77102
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Dr Slobodan Mihaljevic
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Address
77102
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Department of Anesthesiology, Reanimatology and Intensive care medicine
Clinical Center Zagreb
Kispaticeva 12
10 000 Zagreb
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Country
77102
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Croatia
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Phone
77102
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+385915024223
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Fax
77102
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Email
77102
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[email protected]
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Contact person for public queries
Name
77103
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Lada Lijovic
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Address
77103
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Department of Anesthesiology of Obstetrics and Gynecology Clinic
Clinical Hospital Center Zagreb
Petrova 3
10 000 Zagreb
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Country
77103
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Croatia
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Phone
77103
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+385958950935
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Fax
77103
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Email
77103
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[email protected]
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Contact person for scientific queries
Name
77104
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Lada Lijovic
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Address
77104
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Department of Anesthesiology of Obstetrics and Gynecology Clinic
Clinical Hospital Center Zagreb
Petrova 3
10 000 Zagreb
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Country
77104
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Croatia
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Phone
77104
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+385958950935
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Fax
77104
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Email
77104
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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