跳至主要内容
临床试验/CTRI/2024/09/074396
CTRI/2024/09/074396尚未招募不适用

An observational study to evaluate relation of intrapartum VAS scores with postpartum depression

Indira Gandhi Medical College1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年9月29日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
90
试验地点
1
主要终点
To determine the relationship between intrapartum pain relief with incidence of postpartum depression in primigravida females undergoing normal vaginal delivery.

研究概览

简要总结

The labor pain is probably the most severe pain that most women endure in their lifetime.Since pain relief in labor has always been surrounded by myths and controversies, providing effective and safe analgesia in labor have remained a perennial challenge. In the non-obstetric population, the association between chronic pain and depression has been well established.For most women, childbirth is one of the most painful and stressful events during their lives and can result in long-term maternal morbidity. The association between the intensity of childbirth pain and mood disorders, including post-traumatic stress and postpartum depression , in the immediate postpartum period has been proposed, but this association has not been well studied. Central neuraxial analgesia is the gold standard technique for pain relief in labour. Among these, epidural blockade comes close to being the ideal analgesic technique in labour. It provides continuous analgesia for an unpredictable period of time and to convert analgesia to anaesthesia if an operative intervention becomes necessary.After thorough search of literature , we could not find any study that could provide significant evidence that effective labour analgesia could result in decrease in incidence of postpartum depression , hence we would like to proceed with our study of finding relation between intrapartum VAS scores with postpartum depression.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • Primigravida, singleton pregnancy, cephalic presentation with no cpd, gestational age of 37 weeks or more, active stage of labour, normal obstetrics and medical history.

排除标准

  • History of depression/psychiatric illness, multiple gestation, preterm pregnancy, malpresentation, presence of medical complications (preeclampsia, diabetes, neurological disorders), allergy to local anaesthetics, fetal distress.

结局指标

主要结局

To determine the relationship between intrapartum pain relief with incidence of postpartum depression in primigravida females undergoing normal vaginal delivery.

时间窗: 4 week

次要结局

  • To compare patient satisfaction in patients opting for epidural labour analgesia with those opting for normal labour without any analgesia.(Till delivery)

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr DARA SINGH NEGI

Indira Gandhi Medical College

研究点 (1)

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