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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03266432 |
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Date of registration:
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28/08/2017 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Thromboelastometry Guided DIC Prevention After Cesarean Section in Pregnant Women With Placenta Previa
DIC |
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Scientific title:
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Thromboelastometry Guided Disseminated Intravascular Coagulation Prevention After Cesarean Section in Pregnant Women With Placenta Previa |
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Date of first enrolment:
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August 28, 2017 |
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Target sample size:
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60 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT03266432 |
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Study type:
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Interventional |
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Study design:
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Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Prevention. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Egypt
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Contacts
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Name:
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Alaa Mohamed Ahmed Attia, MD |
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Address:
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Telephone:
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01099923117 |
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Email:
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alaa.atya@med.au.edu.eg |
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Affiliation:
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Name:
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ragaa Ahmed Herdan, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Assiut university hopitals |
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Name:
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Mohamed kilany, Master |
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Address:
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Telephone:
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00201090030029 |
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Email:
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mohamedkelany@aun.edu.eg |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- ASA physical status I or II
- Age: = 18 years
- Patients with all types of placenta previa
- Eligible for general anesthesia
- Elective cesarean section
- Singleton term pregnancy
- Normal coagulation profile: prothrombin time (PT), activated partial thromboplastin
time (aPTT), the platelet count, fibrinogen level
Exclusion Criteria:
- Parturient refusal
- Known coagulopathy
- Women with a history of cardiac, respiratory, renal, neurologic or endocrine diseases.
- Eclampsia and preeclampsia
- Emergency surgeries
- Foetal abnormalities
- Drug induced thrombocytopenia as antibiotics
Age minimum:
18 Years
Age maximum:
45 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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DIC Syndrome
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Intervention(s)
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Other: blood samples
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Primary Outcome(s)
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prevention of Postoperative development of DIC
[Time Frame: from time of operation till 48 hours postopertive]
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Secondary Outcome(s)
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prevention of Complications of massive transfusion
[Time Frame: from time of operation till 48 hours postoperative]
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heart rate
[Time Frame: from time of operation till 48 hours postoperative]
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Systolic blood pressure
[Time Frame: from time of operation till 48 hours postoperative]
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diastolic blood pressure
[Time Frame: from time of operation till 48 hours postoperative]
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Secondary ID(s)
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thromboelastometryDIC
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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