跳至主要内容
临床试验/CTRI/2020/04/024740
CTRI/2020/04/024740尚未招募2 期

A randomized single blind comparative clinical study of Bala Taila and Tila Taila yoni pichu and matra basti in sukhprasava

ational Institute of Ayurveda0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • •1.Patient willing and able to participate in study with written informed consent.
  • •2.Pregnant women of age between 20-40 years.
  • •3.Gestational age after 35 weeks.
  • •4.Pregnant women of height 150-170cm.
  • •5.Pregnant women of weight 45-75kg.
  • •6.Hemoglobin more than 10 gm%

排除标准

  • •1.Primigravidae over 35 years of age.
  • •2.Grand multiparae i.e. parity >4.
  • •3.History of previous LSCS along with Bad obstetric history.
  • •4.Pregnancy associated with Pregnancy induced hypertension, Pre-eclampsia, Eclampsia, Gestational Diabetes, Placenta previa, Abruptio placentae.
  • •5.Patients with Cephalo-pelvic disproportion.
  • •6.Patients with any systemic disorder like Diabetes Mellitus, Renal disorder, Cardiac disorder, Tuberculosis, Bronchial asthma.
  • •7.Patients with pathology of Reproductive system like Uterine or Cervical fibroid, Benign or Malignant tumor , Fothergill repair, Recto vaginal fistula, Vesico vaginal fistula, Ovarian cyst.
  • •8.Past history of complication during previous pregnancy or labor like Abruptio placentae,
  • •Postpartum haemorrhage, Intra uterine fetal death.

研究者

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