A study to compare the anaesthetic properties of 0.5% Ropivacaine alone and in combination with Dexmedetomidine for ultrasound guided Supraclavicular brachial plexus block in patients undergoing upper limb surgery. - SCBPB

JLN MEDICAL COLLEGE AJMER0 个研究点目标入组 100 人开始时间: 待定最近更新: 2021年11月24日

试验速览

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•Age group between 15 and 65 years.
•Body weight 30 to 80 kg.
•Patients belonging to ASA (American Society of Anaesthesiologists) class-I and II.
•Patients undergoing upper limb surgeries of duration 1-2 hours in theatre with haemoglobin at least 9 gm/dl.
•Patient free from any associated acute or chronic systemic illness.

•Patients not willing to participate in the study.
•Uncooperative patients.
•Patient with chronic pain or on long-term analgesics.
•Any known hypersensitivity or contraindication to ropivacaine, dexmedetomidine.
•Local pathology at the site of injection or disability limiting the performance of block.
•Patients receiving beta blockers or cardiac drugs.
•History of convulsion, allergy to the drug used, bleeding disorder, severe neurological deficit, thyroid disorder.
•Patient with history of respiratory, cardiac, hepatic or renal disease (necessitating classification in ASA Class III or above).
•Patients having a history of significant neurological, psychiatric, or neuromuscular disorders.
•Pregnant, lactating mothers.
•Inadequate block necessitating institution of general anaesthesia for continuation of surgical procedure.

发起方

JLN MEDICAL COLLEGE AJMER