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Maternal Positioning and Occipitoposterior Fetal Position

Maternal Positioning to Correct Occipitoposterior Fetal Position in Labor: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01291355
Enrollment
438
Registered
2011-02-08
Start date
2011-02-28
Completion date
2014-10-31
Last updated
2014-11-13

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

Conditions

Dystocia, Fetal Position and Presentation Abnormalities, Maternal Distress in Labor, Persistent Occipitoposterior or Occipitoanterior Position

Keywords

Maternal position, Occipitoposterior position, Labor, Dystocia, Fetal presentation Abnormalities

Brief summary

The aim of the study is to evaluate the efficacy of a specific maternal position to correct fetal position in occipito-posterior during the labor. The investigators hypothesize that the maternal position described by the Dr de Gasquet facilitate the rotation in occipito-anterior during the labor. The calculated sample size is 438 participants (219 in each group)

Detailed description

Randomized clinical trial

Interventions

OTHERSpecific maternal position during the labor

women allocated to intervention group will be invited to adopt a posture all fours type:support on the knees, torso tilted forward, back stretched for a minimum of 10 minutes. A cushion is placed between the legs of the woman to limit the cuts.

Sponsors

University of Applied Sciences of Western Switzerland
CollaboratorOTHER
Swiss National Science Foundation
CollaboratorOTHER
University Hospital, Geneva
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 48 Years
Healthy volunteers
Yes

Inclusion criteria

* singleton * primiparous and multiparous * Term ≥ 37 weeks * Labor in dilatation phase (cervix effaced, permeable finger 2 to 9 cm) * Diagnosis of occipitoposterior variety confirmed by ultrasound

Exclusion criteria

* Maternal age below 18 years old * Misunderstanding the French Language * Full dilatation of the cervix * Posture evaluated already adopted by the woman during labor

Design outcomes

Primary

MeasureTime frameDescription
Fetal presentation after the intervention compare to control groupOne hour after the randomization for the studyDiagnosis of the fetal presentation will be measured by an ultra-sound one hour after the randomization in both groups: intervention and control

Secondary

MeasureTime frameDescription
Maternal comfort and pain sensationDuring the hour after the randomizationAuto-administrated questionnaire to assess comfort of the maternal position and pain related to the labor, in intervention group and control group

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026