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Anaesthetic Efficacy of Nalbuphine as an Adjuvant to Ropivacaine in Ultrasound Guided Supraclavicular Brachial Plexus Blockade: A Randomised Controlled Trial UC01-UC04
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Clinical Characteristics and Outcome of Critically ill SARS-CoV-2 Patients Admitted to Intensive Care Unit of a Tertiary Care Hospital in North India: A Retrospective Study UC05-UC08
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Intercostal Nerve Block and Peritubal Infiltration with Bupivacaine for Postoperative Analgesia after Percutaneous Nephrolithotomy: A Randomised Clinical Study UC09-UC12
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A Randomised Blinded Comparison of Epidural Infusion of Ropivacaine and Ropivacaine with Fentanyl for PONV and Sedation in Elective Lower Abdominal Oncosurgeries UC13-UC15
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A Randomised Clinical Trial to Compare the Efficacy of Tramadol and Nalbuphine for Treatment of Shivering after Spinal Anaesthesia in Patients Posted for Lower Limb Orthopaedic Surgery UC16-UC20
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Proseal Laryngeal Mask Gel vs I-gel: A Randomised Clinical Trial among Paediatric Patients UC21-UC25
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Efficacy of Intravenous Fluid Plasmalyte and 6% Hetastarch in Preventing Spinal Anaesthesia Induced Hypotension in Patients undergoing Lower Abdominal Surgeries: A Randomised Clinical Study UC26-UC30
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Effect of Dexamethasone as an Adjunct on Efficacy of Ropivacaine in Caudal Block for Postoperative Analgesia in Paediatric Infra-umbilical Surgeries: A Randomised Double-blind Controlled Study UC31-UC35
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Outcome of Ulinastatin vs Metabolic Resuscitation using Ascorbic Acid, Thiamine and Glucocorticoid in Early Treatment of Sepsis- A Randomised Controlled Trial UC36-UC39
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Airway Management in Hypoxemic Patient using Modified Intubating Laryngeal Mask Airway Technique UL01-UL02
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A Case Series of Lung Sequelae and Aspergillus Antigenemia: A Hidden Entity in Post-COVID-19 Critically ill Patients UR01-UR03
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All the research studies published were performed in accordance to the Declaration of Helsinki. Written consent was obtained from all the included subjects (or the responsible next kin), where ever applicable. In case reports or any article which includes patients images, permission was sought from the patient (or the responsible next kin) for publication. Whether or not this has been explicitly stated in the manuscript, this was declared by the authors at the time of submission of manuscript to the journal. In a rare event, if the consent could not be obtained due to loss of patient for follow up or death or loss of contact, even after reasonable effort, the editors then decided on case by case basis, weighing on the individual contribution the report will make to advancement of medical literature.