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Comparative study of analgesic effect of paracetamol infusion versus intramuscular tramadol injection after gynaecological surgeries: A prospective randomised clinical trial

S. Mirunalini, Subbulakshmi Sundaram, C. Jenitha

International Journal of Clinical Obstetrics and Gynaecology, 2019

30 participants · 1 citation

Abstract

Background: Postoperative pain inadequately treated result in suffering, as well as multiple physiological and psychological consequences which may adversely affect perioperative outcomes and contribute to increased length of stay. Paracetamol a NSAID is an Analgesic and Antipyretic agent. Tramadol an Opioid, has been shown to provide effective analgesia after both intramuscular and intravenous administration for the treatment of postoperative pain. This prospective study is to compare the Analgesic efficacy of intravenous paracetamol and intramuscular tramadol postoperatively. Aims and Objectives: To compare the effect of Paracetamol infusion versus intramuscular Tramadol injection as post operative analgesia after gynaecological surgeries over 48 hours. 1. To compare patients’ demand for analgesia and VAS score at different period of time over 48 hours. 2. To compare the number of doses given over 48 hours including the Rescue Analgesia given in less than 6 hours interval between doses 3. To compare the number of rescue analgesia needed in between the 6 hours interval between doses. Methods: The study was conducted in the Department of Obstetrics and Gynaecology, Rajah Muthiah Medical College and Hospital, Annamalai University, Chidambaram from October 2018 – October 2019 in Gynaecological patients undergoing surgery selecting patients as per the Predetermined Inclusion and Exclusion criteria. and Postoperatively, the calculated doses of, in Group A (n=30) Paracetamol…

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 30 participants or records.

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