Left Lateral Position vs Supine Position to Reduce Active Labor Duration

ConditionLabor Pain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorUniversidad Nacional Autonoma de Honduras

About this trial

This randomized clinical trial aims to compare the effect of the left lateral decubitus position versus the supine position on the duration of the active phase of labor in nulliparous women. A total of 188 participants will be randomly assigned to one of two groups. The intervention group will be placed in the left lateral decubitus position, while the control group will remain in the supine position. Both positions will be maintained for 30-minute intervals with 5-minute rest periods, continuing until delivery. The primary outcome is the duration of the active phase of labor. Secondary outcomes include rates of cesarean section, use of oxytocin and analgesics, and maternal and neonatal complications.

Eligibility criteria

Qualifiers

Signed and dated informed consent form.

Nulliparous woman.

Singleton pregnancy at ≥37 weeks of gestation.

Intact amniotic membranes.

Disqualifiers

Previous uterine surgery.

Maternal condition preventing vaginal delivery.

Fetal anomaly.

Premature rupture of membranes.

Trial design

Treatments tested in this trial

  • Left Lateral Decubitus Group
  • Supine Position Group

Treatment groups

188 Participants
are divided into 2 treatment groups