CTRI/2024/01/061452尚未招募2 期
A clinical comparative Study of Ropivacaine with Dexmedetomidine or Fentanyl as an adjuvant in Thoracic Epidural for patients undergoing abdominal surgeries.
Prashant Singh0 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
- •ASA physical status I and II patients undergoing elective abdominal surgeries.
排除标准
- •1. Age less than 25 years and more than 60 years.
- •2. Unwilling patients not giving consent for operation.
- •3. Emergency cases and cases of duration more than 3 hours.
- •4. ASA physical status class III or more.
- •5. Patients having known hypersensitivity to amide local anaesthetics and Dexmedetomidine.
- •6. Patients displaying sign and symptoms of systemic infection.
- •7. Patients having local infection in thoracic spinal region.
- •8. Patients with pre-existing Diabetes Mellitus, Hypertension, Ischaemic Heart Disease, COPD or any other major systemic illness.
- •9. Pre-existing CNS disorder-Epilepsy and raised intracranial tension.
- •10. Pre-existing respiratory disorder-COPD, Asthma, Chronic Bronchitis.
- •11. Severe renal, hepatic, cardiological, haematological, metabolic disorder.
- •12. Cardiovascular malformation.
- •13. Bleeding diathesis or coagulopathy.
- •14. Spinal deformity.
- •15. Patients on anticoagulant or antiplatelet therapy.
研究者
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