- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04027920
Postpartum Hemorrhage After Shenghua Decoction Treatment
May 31, 2020 updated by: Sheng-Mou Hsiao, Far Eastern Memorial Hospital
Disastrous Delayed Postpartum Hemorrhage After Three Days of Shenghua Decoction Treatment: a Case Report
A rare case of disastrous delayed postpartum hemorrhage after three days of shenghua decoction treatment.
Study Overview
Detailed Description
A rare case of disastrous delayed postpartum hemorrhage after three days of shenghua decoction treatment.
Study Type
Observational
Enrollment (Actual)
1
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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New Taipei
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Banqiao, New Taipei, Taiwan, 22050
- Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital
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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
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
A postpartum woman with delayed pospartum hemorrhage
Description
Inclusion Criteria:
- Postpartum hemorrhage after shenghua decoction treatment.
Exclusion Criteria:
- Nil
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
- Observational Models: Case-Only
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Presence of postpartum hemorrhage or not
Time Frame: 1 year
|
Presence of postpartum hemorrhage or not, following three days of shenghua decoction treatment.
The total estimated blood loss was approximately 2000 mL at that time.
Her hemoglobin was revealed to be 2.6 g/dL, her hematocrit was 8.5%, and the vaginal bleeding persisted despite medications, so emergency total hysterectomy was performed.
|
1 year
|
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)
May 2, 2019
Primary Completion (Actual)
June 17, 2019
Study Completion (Actual)
June 17, 2019
Study Registration Dates
First Submitted
July 12, 2019
First Submitted That Met QC Criteria
July 19, 2019
First Posted (Actual)
July 22, 2019
Study Record Updates
Last Update Posted (Actual)
June 2, 2020
Last Update Submitted That Met QC Criteria
May 31, 2020
Last Verified
July 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 108046-C
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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