Hospital Escuela
Tegucigalpa, Francisco Morazán Department, 11101, Honduras
Location status: Recruiting
NCT Number: NCT07411352
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.
Interested in participating?
Request Info18 year–45 year
Female
Interventional
Not applicable
Tegucigalpa, Francisco Morazán Department, 11101, Honduras
Location status: Recruiting
Globally, maternal positioning during labor is a key component of humanized childbirth. While the World Health Organization recommends allowing women to adopt comfortable positions, the supine position remains prevalent in many clinical settings for practitioner convenience. This study in Honduras seeks to generate local evidence on the impact of maternal position on labor progression. Nulliparous women at term (≥37 weeks) with a singleton pregnancy in cephalic presentation and in the active phase of labor (≥6 cm dilation) will be recruited from the labor and delivery unit of the Hospital Materno Infantil. After providing informed consent, participants will be randomized. The primary efficacy endpoint is the time from the onset of the active phase (or intervention start, if later) until delivery. The study hypothesizes that the left lateral position will significantly reduce active labor duration compared to the supine position, potentially reducing unnecessary surgical interventions and improving the childbirth experience.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will be placed in the left lateral decubitus position for periods of 30 minutes, interspersed with 5-minute rest periods. This cycle will continue throughout the active phase of labor until delivery.
Participants will remain in the supine position for periods of 30 minutes, interspersed with 5-minute rest periods. This cycle will continue throughout the active phase of labor until delivery.
Time frame: Time (in minutes) from the diagnosis of the active phase of labor (cervical dilation ≥6 cm) to delivery of the newborn. Within the first 24 hours after diagnosis of active phase.
The primary objective is to measure and compare the time taken to progress from the active phase to delivery between the two positioning groups.
Time frame: From randomization until delivery (anticipated within 48 hours per participant).
The proportion of participants in each group who undergo a cesarean section.
Time frame: From randomization until delivery.
The proportion of participants in each group who receive oxytocin infusion.
Time frame: From randomization until hospital discharge (approximately 24-48 hours postpartum).
Composite of adverse maternal outcomes recorded during labor and the immediate postpartum period.
Time frame: At 1 minute and 5 minutes after birth.
The Apgar score (0-10) will be recorded and compared between groups.
Interested in participating?
Request InfoUniversidad Nacional Autonoma de Honduras
Other
Left Lateral Position Versus Supine Position in Reducing the Duration of the Active Phase of Labor: A Randomized, Single-Blind Clinical Trial
Acronym: DLI-SP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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