Evaluation of the effectiveness of Tadalafil on improving pulmonary function and asthma severity in severe asthmatic patients: a randomized controlled trial study.

IF 1.1 Q4 RESPIRATORY SYSTEM
Monaldi Archives for Chest Disease Pub Date : 2025-03-31 Epub Date: 2024-01-11 DOI:10.4081/monaldi.2024.2685
Seyed Hamid Borsi, Seyed Ali Asghar Fakhr Mousavi, Mehrdad Dargahi Mal-Amir, Heshmatollah Tavakol, Hanieh Raji
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引用次数: 0

Abstract

Phosphodiesterase inhibitors elevate the levels of cyclic adenosine monophosphate and cyclic guanosine monophosphate, which have been associated with various anti-inflammatory effects that can help alleviate asthma symptoms. This study aims to assess the impact of Tadalafil, a selective phosphodiesterase inhibitor, on pulmonary function in patients with asthma. This study was a randomized, double-blind clinical trial conducted in 2021 at Imam Khomeini Hospital in Ahvaz, Iran. The study enrolled 44 patients with severe asthma, who were divided equally into a Tadalafil group and a placebo group. The Tadalafil group received 20 mg/day of Tadalafil, while the placebo group received a placebo at the same dose. The patients' spirometry tests, asthma quality of life questionnaire, 6-minute walking distance, and quality of life were measured at the beginning of the study and one month later. The study results indicated that there was no statistically significant difference between the Tadalafil group and the placebo group in terms of pulmonary parameters (p>0.05). Furthermore, the scores for patients' quality of life (p=0.167) and the 6-minute walking test (p=0.148) at the end of the study did not show any statistically significant improvement compared to the placebo group. Results showed that the use of Tadalafil (20 mg) once daily for one month in patients with severe asthma did not affect clinical and laboratory outcomes.

评估他达拉非改善严重哮喘患者肺功能和哮喘严重程度的效果:随机对照试验研究。
磷酸二酯酶抑制剂能提高环磷酸腺苷和环磷酸鸟苷的水平,而这两种物质具有多种抗炎作用,有助于缓解哮喘症状。本研究旨在评估选择性磷酸二酯酶抑制剂他达拉非对哮喘患者肺功能的影响。这项研究是一项随机双盲临床试验,于 2021 年在伊朗阿瓦士的伊玛目霍梅尼医院进行。研究共招募了 44 名重症哮喘患者,将他们平均分为他达拉非组和安慰剂组。他达拉非组每天服用 20 毫克他达拉非,安慰剂组服用相同剂量的安慰剂。研究开始时和一个月后,对患者的肺活量测试、哮喘生活质量问卷、6 分钟步行距离和生活质量进行了测量。研究结果表明,在肺部参数方面,他达拉非组与安慰剂组之间的差异无统计学意义(P>0.05)。此外,研究结束时患者的生活质量评分(P=0.167)和 6 分钟步行测试(P=0.148)与安慰剂组相比也没有出现统计学意义上的明显改善。结果表明,严重哮喘患者使用他达拉非(20 毫克),每天一次,持续一个月,不会影响临床和实验室结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
1
审稿时长
12 weeks
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