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Clinical Implications of Fetal Positioning During Delivery

Clinical Implications of Fetal Positioning During Delivery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04813237
Enrollment
300
Registered
2021-03-24
Start date
2021-03-31
Completion date
2021-12-30
Last updated
2021-04-30

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

Conditions

Fetal Position and Presentation Abnormalities

Keywords

fetal malposition, fetal left occiput position, fetal right occiput position

Brief summary

The project aims to find a relationship between the positioning of the foetus before and during birth and the results of obstetrics and to determine their incidence in the Polish population. The study will be conducted by combining the use of ultrasound diagnostics, midwives observations during childbirth, analysis of medical documentation and a questionnaire on the activity of examined women. The obtained results will be used to prepare guidelines for the birth in a particular foetus position.

Detailed description

The purpose of the examination is to describe the difficulties associated with delivery in a non-optimal position of the fetus. Initial observations show that such childbirth is perceived as difficult by both the women giving birth and the staff. The aim of the study is to describe the level of difficulty of this labor, expressed as the experience of the woman, as well as all the elements that may affect the difficulty of this labor, for example, slower or no progress in labor, disturbances in systolic function, injuries, the need to use epidural anesthesia, increased blood loss.

Interventions

OTHERn a

the participants are not subjected to any type of intervention

Sponsors

Foundation for St. Sophia Specialist Hospital in Warsaw
CollaboratorUNKNOWN
Żelazna Medical Centre, LLC
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* during childbirth, * in a single pregnancy,

Exclusion criteria

* pelvic position of the fetus * in whom labor is induced for reasons other than post-term pregnancy, * women who came to the hospital in the second stage of labor * severe diseases mother or foetus.

Design outcomes

Primary

MeasureTime frameDescription
Mode of deliveryimmediately after deliveryMode of delivery as measured by number of women who had a vaginal, instrumental or operational delivery.

Secondary

MeasureTime frameDescription
Uterine contractionsduring birthuterine contractions as measured by number of contractions and assessment of uterine contractile coordination
Labor progressduring birthLabor progress as measured by assessment of the head insertion, advancement in the birth canal,
Epiduralimmediately after deliveryas measured by epidural or not
Perineum injuryimmediately after deliveryas measured by number and extent of injury
Duration of deliveryimmediately after birththe time of 1,2,3 and 4 stage of labor
Methods of placental separationimmediately after deliveryas measured by number of Duncan or SchultZ methods
Blood lossimmediately after deliverypostpartum blood loss (ml)
Difficulty of childbirthimmediately after deliverydifficulty of childbirth as measured by subjective assessment of the woman and the midwife
Episiotomyimmediately after deliveryas measured by episiotomy or not

Countries

Poland

Contacts

Primary ContactMagdalena Witkiewicz, BA
magdawitkiewicz@o2.pl603 404 799

Outcome results

None listed

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