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临床试验/NCT06069596
NCT06069596已完成4 期

Evaluation of the Effectiveness of Obstetric Lubricant Gel in Labor in Nulliparous and Primiparous Women: A Randomized Controlled Study

Ankara University0 个研究点目标入组 220 人开始时间: 2017年1月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
220
主要终点
The duration of the second stage of labor was compared between the study and control groups

研究概览

简要总结

The investigators hypothesized that the application of lubricant gels at the beginning of the active phase of the labor may reduce duration of the delivery and episiotomy rates. The aim of this study is to investigate and confirm this hypothesis through a randomised controlled trial.

All participants in the study received standard routine antepartum care in the delivery room. Obstetric lubricant gel was applied to patients in the study groups, which had 47 nulliparous and 50 primiparous patients. Perinatal outcomes were compared between the groups.

详细描述

The participants were divided into two groups based on their parity: nulliparous and primiparous. Initially, each group had 110 participants. Nulliparous and primiparous groups were randomly assigned to two groups as study and control groups using a computer-generated random number table. In this randomized controlled trial, participant allocation was carried out using a computer program to ensure a randomized and unbiased selection process. The randomization procedure was conducted in a double-blind manner, with the study investigators remaining unaware of the allocation until the conclusion of the study. All participants in the study received standard routine antepartum care in the delivery room. Among all patients, 25 participants were lost to follow-up during the study. Consequently, obstetric lubricant gel was applied to patients in the study groups, which included 47 nulliparous and 50 primiparous patients. Perinatal outcomes were compared between the groups

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Care Provider, Investigator, Outcomes Assessor)

盲法说明

Randomization was performed using a computer program. Accordingly, the study group patients were administered Obstetric gel. The researcher administering Obstetric gel ensured the blinding of healthcare providers and other researchers.

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Nulliparous and primiparous singleton pregnancies between 37 and 41 weeks + six days of gestation and vertex presentation of fetus with an estimated birth weight of 2000 - 4500g were included in the study

排除标准

  • Multiparous pregnancies and women who had ceserean section before and/or contraindication for vaginal delivery were excluded from the study.

结局指标

主要结局

The duration of the second stage of labor was compared between the study and control groups

时间窗: 0 to 240 minutes

The second stage of labor begins when the cervical dilation is complete and continues until the birth of the newborn.

The duration of the active phase of the first stage of labor was compared between the study and control groups

时间窗: 0 to 600 minutes

The active phase of labor begins when the cervical dilation is between 4-6 cm and refers to the time elapsed until full cervical dilation.

次要结局

  • Episiotomy rates(Episiotomy is a technique performed during the second stage of labor.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

kaan baydemir

Investigator

Ankara University

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