Comparison of analgesic efficacy of Intravenous Dexamethasone and Intravenous Paracetamol for post-surgical pain in elective caesarean sections - A randomised double blinded study

Dr Snigdha Bellapukonda0 个研究点目标入组 0 人开始时间: 待定最近更新: 2021年11月24日

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•After approval of our Institutional Ethical Committee and obtaining informed consent. American Society Anesthesiologists (ASA) II pregnant patients posted for elective Caesarean section of age 18-35 years will be enrolled in the study with height >140cm.

•Pregnant patients with
•I. Diabetes mellitus
•II. Chorioamniotis
•III. Preeclampsia
•IV. Pregnant women having contraindication to spinal anaesthesia, those who have accompanying, placenta praevia, and twin pregnancy, those whose weight will be < 50 kg or > 100 kg, height < 140 cms those with cardiopulmonary disease, cerebrovascular diseases, autonomic neuropathy, spinal deformities, other neurological diseases, infections in the lumbar area, coagulation abnormalities, hypovolemia due to any cause and systolic blood pressure (SBP) < 100 mmHg, fetal distress will be excluded from the study. Patients with placental complications (placenta praevia or placental abruption), cord complications (nuchal cord or cord prolapse), fetal malformations, premature deliveries. All other patients requiring emergency cesarean sections. Patients already on chronic steroid use.
•V. All cesarean sections planned for or converted to General Anesthesia.

发起方

Dr Snigdha Bellapukonda