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Analyzes of Hemorrhagic Obstetric Patients Whose Were Used Fibrinogen

Treatment of Obstetric Hemorrhage With Fibrinogen and Blood Products: Retrospective Analyzes

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03723200
Enrollment
56
Registered
2018-10-29
Start date
2018-10-09
Completion date
2018-10-24
Last updated
2018-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemorrhage

Keywords

Hemorrhagic, Obstetric, Fibrinogen

Brief summary

The files of hemorrhagic obstetric patients undergoing surgery and followed in the intensive care unit and using Fibrinogen and blood products were included in the study between January 2015- September 2018 at the Anesthesiology and Reanimation Clinic of SBU Kanuni Sultan Süleyman Training and Research Hospital. Patients under 18 years of age were excluded from the study. In this study, ages, operation types, number of blood and products, the amount of fibrinogen, the results of the hemogram and bleeding parameters, the levels of fibrinogen, the duration of hospital stay and the intensive care unit were recorded.

Detailed description

Bleeding is an important event that threatens the patient's life. Too much blood and blood products can be used in massive bleeding. However, unwanted allergic reactions may occur in blood and blood product transfusions. Fibrinogen is the first coagulation factor in coagulopathy. Some studies have shown that when the fibrinogen level falls to \<150-200 mg / dl, the bleeding increases dramatically.

Interventions

OTHERFibrinogen and blood products

Fibrinogen and blood products

Sponsors

Kanuni Sultan Suleyman Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years

Inclusion criteria

* Obstetric patients, underwent surgery and followed in ICU * Used Fibrinogen and Blood products * Over 18 years age

Exclusion criteria

* Under 18 years age * Obstetric patients, underwent surgery but not used Fibrinogen and Blood products

Design outcomes

Primary

MeasureTime frameDescription
Amount of blood products (unit)24 hoursdegree of hemorrhagie
Measurement of hemoglobin (g/dL)24 hoursPostpartum hemorrhage (PPH) is a major contributor to maternal death and severe maternal morbidity
Amount of fibrinogen consantrates24 hoursin order to avoid PPH
Measurement of fibrinogen (mg/L)24 hoursSignificant independent predictor for evolution to severe PPH was plasma fibrinogen level.

Secondary

MeasureTime frameDescription
Hospital stay days24 hoursfor the recovery time of patients

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026