跳至主要内容
临床试验/CTRI/2024/07/070837
CTRI/2024/07/070837尚未招募2 期

Randomized Controlled Trail Comparing Ropivacaine 0.125% and Ropivacaine 0.2% in Conjunction With Fentanyl For Continuous Epidural Infusion In Antenatal Patients Experiencing Active Labor: An Assessment of Labor Pain Management. - NI

Priti Mourya0 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. Singleton pregnancy at term (=37 weeks of
  • gestation) with vertex presentation.
  • 2. Maternal age should be between 19 and 35 years.
  • Because according to child marriage act the age
  • of marriage for girls is 18 years and age =35
  • years is very advanced maternal age with
  • complicated outcomes like stillbirth, preterm
  • birth, perinatal death, GDM, gestational
  • hypertension and preeclampsia.
  • 3. Informed consent provided by the participant.
  • 4. Desire for epidural analgesia for pain
  • management.
  • 5. Ability to understand and comply with the study
  • procedures.

排除标准

  • 1. Refusal to provide informed consent.
  • 2. Twin pregnancy.
  • 3. Breech presentation.
  • 4. Pregnancy with antepartum haemorrhage.
  • 5. History of adverse reactions to local
  • anaesthetics or opioids.
  • 6.Medical contraindications to epidural
  • analgesia like increased intracranial pressure,
  • local infection at the site of puncture,
  • haemorrhagic diathesis or
  • therapeutic anticoagulants.
  • 8. Known foetal anomalies or distress
  • necessitating
  • immediate delivery.
  • 9. History of drug abuse.
  • 10. Bleeding disorders.
  • 11. Decreased platelet counts.
  • 12. Spinal column deformities.
  • 13. History of spine surgery.

研究者

发起方
Priti Mourya

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