- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04160923
Incidence and Neonatal Outcome of Eclamptic Parturient in Tertiary Hospital.
November 13, 2019 updated by: Pattrapun Wongsripuemtet, Siriraj Hospital
Incidence and Neonatal Outcome of Eclamptic Parturient : a 13-years Retrospective Study From a Single Tertiary Care Center Anesthetic Aspect.
Eclampsia is a rare but serious disease that can happen during the pregnancy.
Both general and regional anesthesia can both be performed in eclamptic patients.
Eclamptic patients has greater risk if undergo general anesthesia such as risks associated with general anesthesia in pregnancy and also cerebral hemorrhage risks from hypertension during laryngoscope application and thrombocytopenia that can happen in eclamptic patients.
So, most of Anesthesiologists tend to avoid performing general anesthesia in these patients.
But spinal anesthesia also has side effects such as hypotension or epidural hematoma.
And nowadays there's minimal evidence on suitable anesthesia in eclamptic patients.
Our study wants to review on how choice of anesthesia affects these patients both mothers and their neonates
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
46
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
-
-
Bangkok
-
Bangkok Noi, Bangkok, Thailand, 10700
- Department of Anesthesiology, Siriraj Hospital, Mahidol University
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Bangkok Noi, Bangkok, Thailand, 10700
- Pattrapun Wongsripuemtet
-
-
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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Patient who diagnosed with eclampsia during January2005-December 2017
Description
Inclusion Criteria:
- Patient who diagnosed with eclampsia.
Exclusion Criteria:
- Incomplete medical record.
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 incidence of eclampsia in Siriraj Hospital.
Time Frame: 13 years
|
Incidence represent as percent.
|
13 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Soawaphak Chumpathong, Assoc. Prof., Department of Anesthesiology, Siriraj Hospital, Mahidol University
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)
May 1, 2016
Primary Completion (ACTUAL)
April 1, 2019
Study Completion (ACTUAL)
May 1, 2019
Study Registration Dates
First Submitted
November 10, 2019
First Submitted That Met QC Criteria
November 10, 2019
First Posted (ACTUAL)
November 13, 2019
Study Record Updates
Last Update Posted (ACTUAL)
November 15, 2019
Last Update Submitted That Met QC Criteria
November 13, 2019
Last Verified
November 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SIRB 390/2017
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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