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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04027920
Other study ID # 108046-C
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2, 2019
Est. completion date June 17, 2019

Study information

Verified date July 2019
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A rare case of disastrous delayed postpartum hemorrhage after three days of shenghua decoction treatment.


Description:

A rare case of disastrous delayed postpartum hemorrhage after three days of shenghua decoction treatment.


Recruitment information / eligibility

Status Completed
Enrollment 1
Est. completion date June 17, 2019
Est. primary completion date June 17, 2019
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Postpartum hemorrhage after shenghua decoction treatment.

Exclusion Criteria:

- Nil

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Shenghua Decoction
Three days' shenghua decoction treatment

Locations

Country Name City State
Taiwan Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital Banqiao New Taipei

Sponsors (1)

Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Presence of postpartum hemorrhage or not 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
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