Camylofin 50 mg and Paracetamol 325 mg in patients with acute colicky abdominal pain: a prospective and open-label study

Authors

  • Chandravati Krishna Medical Centre, I-Rana Pratap Marg, Hazratganj, Lucknow, Uttar Pradesh, India

DOI:

https://doi.org/10.18203/2320-1770.ijrcog20243934

Keywords:

Abdominal colic, Camylofin, Paracetamol

Abstract

Background: Acute colicky abdominal pain (AP), resulting from the sudden spasm of hollow viscera, is frequently managed with a combination of analgesics and antispasmodics. Camylofin is an anti-spasmodic medication whereas paracetamol is a widely prescribed analgesic and antipyretic for managing mild-to-moderate pain. This study evaluates the effectiveness of a fixed-dose combination (FDC) of camylofin 50 mg and Paracetamol 325 mg in alleviating acute colicky abdominal pain.

Methods: In this prospective, single-arm, open-label study, 100 female patients aged 18-65 with acute colicky abdominal pain were administered one tablet thrice daily for 3-5 days of camylofin 50 mg and paracetamol 325 mg daily for 3-5 days. Pain intensity was assessed using the visual analog scale (VAS) at baseline, Day 3 and Day 5.

Results: A significant reduction was observed in the mean VAS scores from baseline (77.8) to Day 5 (4.0) (p<0.001). At day 5, 83.0% of patients reported no pain, with minimal adverse events (2% fever and 1% headache with fever). There was a significant change (-27.5) in mean pain intensity VAS score before (77.8) and after (50.2) medication, p<0.001. The percentage change in the mean pain intensity based on VAS score was highest in subjects with urinary AP (97.4%), followed by menstrual AP (94.9%) and unexplained AP (94.5%). 

Conclusions: The FDC of camylofin 50 mg and Paracetamol 325 mg is significantly effective in managing acute colicky abdominal pain, providing rapid and substantial pain relief with minimal adverse events.

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Published

2024-12-27

How to Cite

Chandravati. (2024). Camylofin 50 mg and Paracetamol 325 mg in patients with acute colicky abdominal pain: a prospective and open-label study. International Journal of Reproduction, Contraception, Obstetrics and Gynecology, 14(1), 111–116. https://doi.org/10.18203/2320-1770.ijrcog20243934

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Original Research Articles