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Retrospective Evaluation of the Impact of Epidural on the Risk of Postpartum Hemorrhage

Retrospective Evaluation of the Impact of Epidural on the Risk of Postpartum Hemorrhage

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06816654
Enrollment
5753
Registered
2025-02-10
Start date
2023-12-12
Completion date
2024-05-22
Last updated
2025-02-10

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

Conditions

Postpartum Hemorrhage

Keywords

Epidural anesthesia, Postpartum hemorrhage, Obstetric analgesia, Neuraxial anesthesia, Instrumental delivery, Obstetrical trauma

Brief summary

Postpartum hemorrhage (PPH) is a major complication of childbirth. Epidurals are often implicated in the onset of postpartum hemorrhages. Given the paradoxical data in the literature, the investigators wished to retrospectively evaluate the impact of epidurals on the risk of PPH, instrumental delivery and the occurrence of PPH risk factors. The investigators retrospectively analyzed 5753 records of patients who gave birth vaginally at Brugmann University Hospital between January 1, 2020 and December 31, 2021. The primary objective was to assess whether epidurals pose a risk of postpartum hemorrhage. Secondly, the investigators assessed whether epidurals pose a greater risk of instrumentation of delivery and emergence of PPH risk factors.

Interventions

OTHERData extraction from medical records

Data extraction from medical records

Sponsors

Tatiana Besse-Hammer
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who gave birth vaginally at the Brugmann University Hospital Horta site between January 1, 2020 and December 31, 2021.

Exclusion criteria

* Patients who gave birth before 25 weeks. * Patients who gave birth outside of hospital. * Patients who had recourse to a medical termination of pregnancy (MTP). * Patients who gave birth by cesarean section.

Design outcomes

Primary

MeasureTime frameDescription
Postpartum blood lossUp to 24 hours after the birth of the babyTotal blood loss is analyzed according to a standardized protocol: use of the calibrated field of the collection bag and of a precision scale to weigh the blood soaked compresses

Secondary

MeasureTime frameDescription
PPH risk factorsData extraction in medical files from January 1st 2020 till December 31th 2021Presence/absence of one or more PPH risk factors (yes/no) such as : uterine atony, placental abnormalities, obstetric trauma, and coagulopathy.

Countries

Belgium

Outcome results

None listed

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