Skip to content

Evaluation of the Impact of Ambulatory Epidural on Maternal Satisfaction During Delivery and Postpartum

Evaluation of the Impact of Ambulatory Epidural on Maternal Satisfaction During Delivery and Postpartum

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06550570
Acronym
PERIDEAMBU
Enrollment
126
Registered
2024-08-13
Start date
2024-07-23
Completion date
2026-08-23
Last updated
2026-06-24

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

Conditions

Childbirth, Epidural; Anesthesia

Keywords

Maternal satisfaction, ambulatory epidural, physiology, analgesia

Brief summary

Childbirth is a special event for women. Maternal satisfaction regarding childbirth is quite important, that is why this factor has to be taken into account. A bad experience related to childbirth could lead to serious psychological and organic consequences such as postpartum depression, mother-baby bond deterioration and chronic pelvic pain. Childbirth image changed over the years to the extent that an increasingly physiological process keeping analgesia and safety is more and more desired. In this perspective, this study aims to investigate an approach so-called ambulatory epidural. Indeed, only a few studies have been conducted and the ones published in 1990s did not involve the current recommended pharmacological protocols.

Detailed description

This is a multi-centre prospective observational analytical before/after-type study. Practice changes are planned in concerned departments, in particular regarding usual patient care. This observational study aims to quantify the impact of practice changes on patient experience using a Childbirth Assessment Questionnaire (QEVA). During the "before" period, patients will receive a conventional epidural while the others, during the "after" period, will receive an ambulatory epidural. The women involved into this study must fill the QEVA form 2 days after giving birth (at the maternity) then 4 weeks after giving birth in order to get a feedback related to postpartum feelings (phone call).

Interventions

BEHAVIORALQEVA questionnaire

QEVA questionnaire administered at 2 days pospartum (in hospital) and 4 weeks postpartum (phone call). (specific for the study)

Sponsors

Centre Hospitalier Régional Metz-Thionville
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Women older than 18 years old * with Physiological pregnancy (fetus cephalic position, normal fetal heart rate, spontaneous work between 37 and 41 SA) * Having benefited from epidural, usual or ambulatory depending on the study period * who speeks and understand French * who signed a free and informed consent form

Exclusion criteria

* Hearing or comprehension impairment * Twin pregnancies * Scarred uterus * Fetus in non cephalic position * Imminent delivery * Women under protective supervision (guardianship, curatorship) * Women bereaved of a spouse or child during pregnancy * Hospitalization of child in neonatology after delivery * Women hospitalized in critical care units after childbirth

Design outcomes

Primary

MeasureTime frameDescription
Obstetrical labor and delivery experience in birthgiving womenat 2 days postpartumThe "emotional state" dimension of the Childbirth Assessment Questionnaire (QEVA) will be evaluated. This questionnaire is written and validated in French. It contains 26 questions covering 4 dimensions: emotional state, relations with nursing staff, first moments with the baby, and the young mother's feelings one month before delivery.

Secondary

MeasureTime frameDescription
Relations with nursing staff and first moments with the childat 2 days postpartumOther dimensions and isolated items of the QEVA questionnaire
Obstetrical labor and delivery experience in birthgiving womenat 4 weeks postpartum" emotional state " dimension of the Childbirth Assessment Questionnaire (QEVA)
Labor and delivery safety : time spent in the delivery roomat 2 days postpartumTime spent in the delivery room (min)
Labor and delivery safety: need for instrumental extractionat 2 days postpartumNeed for instrumental extraction (yes/no)
Labor and delivery safety : emergency caesarean sectionsat 2 days postpartumEmergency caesarean sections (yes/no),
Labor and delivery safety: ability to maintain spontaneous micturitionat 2 days postpartumAbility to maintain spontaneous micturition (yes/no)
Safety of ambulationat 2 days postpartumabsence of the following events : motor block, hypotension, malaise, falls, difficulty in achieving ambulation

Countries

France

Contacts

CONTACTArpiné EL NAR, PhD
projet-recherche-clinique@chr-metz-thionville.fr0033387557766
CONTACTMélanie JUNKE
projet-recherche-clinique@chr-metz-thionville.fr
PRINCIPAL_INVESTIGATORLisa LEON, MD

CHR Metz Thionville Hopital Femme Mère Enfant

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 25, 2026