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临床试验/CTRI/2022/12/048237
CTRI/2022/12/048237尚未招募4 期

Comparison Of Pain Relief In Tranversus Abdominus Plane Block In Patients Undergoing Laparoscopic General Surgery Using 20 Ml Of 0.25% Bupivacaine Verses 19 Ml Of 0.25% Bupivacaine And 1Ml Methylene Blue

SIR H.N RELIANCE FOUNDATION HOSPITA0 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

  • PATIENTS GIVING INFORMED VALID CONSENTS
  • PATIENTS UNDERGOING LAPAROSCOPIC SURGERY UNDER GENERAL ANAESTHESIA

排除标准

  • 1)PATIENTS UNWILLING TO GIVEN CONSENT
  • 2) AGE LESS THAN 18 YEARS OR MORE THAN 70 YEARS
  • 3) DOCUMENTED ALLERGY OR INTOLERANCE TO STUDY COMPOUND
  • 4) ANY SEVERE PERI-OPERATIVE COMPLICATIONS
  • 5) PATIENTS ON CHRONIC PAIN MEDICATIONS
  • 6) INTRA-OPERATIVE CONVERSION FROM LAPAROSCOPIC TO OPEN
  • 7) PREGNANCY OR LACTATING MOTHERS
  • 8) CO-EXISTNG SEVERE CARDIOVASCULAR, NEUROLOGICAL, HEPATIC, RENAL OR ENDOCRINOLOGICAL DISTURBANCES.

研究者

发起方
SIR H.N RELIANCE FOUNDATION HOSPITA

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