跳至主要内容
临床试验/CTRI/2023/06/053883
CTRI/2023/06/053883尚未招募2 期

A Randomized Comparative clinical study to evaluate the efficacy of Integrated and Individual approaches in achieving Sukhaprasava

ational Institute of Ayurveda Deemed to be university0 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
发起方

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 with37 weeks of gestation with cephalic presentation.
  • 2. Height 148 cm to 172 cm.
  • 3. Haemoglobin more than or equal to 10 gm%.
  • 4. Borderline or adequate pelvis

排除标准

  • 1. History of previous LSCS less than or equal to 3 years.
  • 2. Patient having bad obstetric history, precious pregnancy.
  • 3. Pregnancy associated with severe Pregnancy induced hypertension, pre-eclampsia, eclampsia, gestational diabetes, placenta previa (2nd grade posterior, 3rd and 4th grade), abruptio placentae, severe oligohydramnios, severe polyhydramnios, severe IUGR.
  • 4. Patients with cephalo-pelvic disproportion, malpresentation.
  • 5. Patients suffering with systemic disorders like diabetes mellitus, renal dysfunction, cardiac disorder, tuberculosis, coagulopathies.
  • 6. Patients diagnosed with benign or malignant tumor of reproductive system, recto vaginal fistula, vesico-vaginal fistul, second and third degree uterine prolapse.
  • 7. History of fothergill repair, recto vaginal fistula, vesico-vaginal fistul.
  • 8. VDRL, HIV, HBsAg positive pregnant woman.

研究者

发起方
ational Institute of Ayurveda Deemed to be university

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