View clinical trials related to Post-operative.
Filter by:The study design will be double blinded retrospective controlled comparative study. The patients will be included in the study shoud be in the following category: - American Society of Anesthesiologists (ASA) physical status I, II - Age range from 18 and 70 years. The patients will be discarded from the study shoud be in the following: - patient refusal. - significant renal, hepatic and cardiovascular diseases. - Pregnancy. - Any contraindication to regional anesthesia such as local infection or bleeding disorders. - Chronic opioid use, history of chronic pain and cognitive disorders. - Lumbar spine lesion revision and dural tear. Postoperative pain will be evaluated using a visual analogue scale (VAS) score as primary outcome measure. demographic data ( Age, Weight, sex and height) , ASA classification ,mean operative times (min), time to the first rescue analgesic (min) ,intraoperative fentanyl consumption(microgram),postoperative opioid consumption ,sedation score, hemodynamics intraoperative and postoperative ( BP ,H R and oxgen saturation %) and complications as 2ry outcome measures.
The aim of this study is to measure and compare the effectiveness of nanosilver combined calcium hydroxide and conventional calcium hydroxide intracanal medications in reducing postoperative pain in patients with Symptomatic Root Canal treatment Failure .
This study seeks to investigate the prescribing patterns and patient utilization of opioid pain medication in the postpartum setting. Postpartum women will be surveyed prior to hospital discharge and again at 2-4 weeks postpartum in order to assess the number of opioid tablets they used (in relation to the number prescribed), pain satisfaction, and storage/disposal of any remaining opioid tablets.