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临床试验/CTRI/2022/04/041914
CTRI/2022/04/041914尚未招募2 期

A comparative study of labour analgesia between epidural analgesia and combined spinal epidural analgesia using bupivacaine and fentanyl in primiparous parturients.

Rajendra Institute of Medical Sciences Ranchi0 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. Only booked primigravida parturient with all antenatal investigations within normal limits.
  • 2. ASA physical status I and II.
  • 3. Age group between 18-35 years.
  • 4. Height > 140 cms.
  • 5. Patients with full term singleton pregnancy (gestational age between 37-42 weeks) in active phase of first stage of labour with good uterine contractions and cervical dilatation 3-5 cm with vertex presentation.
  • 6. Cervical dilation >3 cm and <5 cm.

排除标准

  • 1. ASA grade III and IV.
  • 2. Age <18 years or >35 years.
  • 3. Preterm gestation.
  • 4. Patients who did not give consent.
  • 5. Patient with severe anaemia, bleeding disorders, coagulation abnormalities or on anticoagulant therapy or history of prolonged aspirin ingestion.
  • 6. Patients with spine deformity.
  • 7. Patients with history of spine surgery.
  • 8. Patient with history of chronic backache.
  • 9. Patients with pre-existing neurological or spinal disease, cardiovascular or respiratory impairment, local or systemic infection, cephalopelvic disproportion, feto placental insufficiency.
  • 10. Fetal distress.

研究者

发起方
Rajendra Institute of Medical Sciences Ranchi

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