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临床试验/CTRI/2019/07/020098
CTRI/2019/07/020098尚未招募4 期

Clinical Evaluation of Efficacy and Safety of Transversus Abdominis Plane Block with Inj. Levobupivacaine v/s Inj. Ropivacaine for Post Operative Analgesia following Lower Segment Cesarean Section: A Prospective, Randomised, Double Blind Study

Department of Pharamcology0 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
4 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. Informed written consent for participation in study.
  • 2. Age: 20 to 35 years
  • 3. Antenatal female patients scheduled for lower segment cesarean scetion.
  • 4. Primi patients undergoing LSCS d/t CPD, Diabetes, Placenta Previa.
  • 5. Singleton pregnancy
  • 6. ASA physical status 1 and 2

排除标准

  • 1. Patient refusing consent.
  • 2. Multiple pregnancy
  • 3. Mutipara
  • 4. Neuropsychiatric disorder
  • 5. Patient having post partum psychosis.
  • 6. Allergy or hypersensitivity to local anesthetic or NSAIDS.
  • 8. Patient on any form of analgesics therapy.
  • 9. Patient on ECG showing QT prolongtion.
  • 10. ASA pysical status 3 and 4.
  • 11. Contraindication to spinal anesthesia
  • - Local infection or sepsis at site of Lumbar Puncture.
  • - Bleeding disorders, thrombocytopenia
  • - Space occupying lesons of the brain.
  • - Anatomical disorder of spine
  • - Hypovolemia e.g. following massive hemorrhage

研究者

发起方
Department of Pharamcology

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