Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.
Headache. 2024 Nov-Dec;64(10):1285-1297. doi: 10.1111/head.14828. Epub 2024 Sep 9.
Fasting headaches frequently occur during the first few days of Ramadan, and treatment is challenging because of fasting.
This study aimed to evaluate the effect of extended-release paracetamol on preventing fasting headaches.
A randomized, open-label clinical trial investigated the efficacy of extended-release paracetamol at a daily dose of 1330 mg in preventing fasting headache. Adults aged 18 years and older were recruited through the Clinical Trial Unit at the King Saud University Medical City. The eligible participants in the study fasted 13.5 h daily during the first week of Ramadan. Participants in the treatment and control arms were followed up to investigate the occurrence, severity, and timing of headache symptoms via self-reporting using a standardized headache diary scale with a daily online link or phone call. The primary outcome was the frequency of headache episodes while fasting during the first week of Ramadan.
A total of 238 participants were enrolled and randomized. Of these, 173 followed the protocol (80 treated, 93 control) for at least the first day and were included in the analysis. Most participants were young and healthy, with a mean age of 32.2 ± 10.2 years. More men were included in the study (102/173; 59.0%), a small proportion of participants were smokers (31/173; 17.9%), and almost all participants reported being coffee drinkers (165/173; 95.4%); nonetheless, these characteristics were evenly distributed between the two groups in the study. The overall incidence of headache episodes was 33.0% (57/173) on day 1 and decreased to 11.3% (18/159) on day 7. On average over the 7 days, no significant effect was observed for the treatment on the incidence of headache, as the findings from the generalized estimating equation model indicated (β = -0.398, p = 0.084; odds ratio = 0.67, 95% confidence interval [CI] 0.42-1.06). Moreover, there was initially no significant difference in the incidence of headache episodes between the treatment and control groups. However, the treatment group had significantly fewer headache episodes during fasting than the control group on day 3 (4/72 [5.6%] vs. 15/91 [16.5%], p = 0.031; relative risk [RR] = 0.34, 95% CI 0.12-0.97) and day 6 (5/69 [7.2%] vs. 20/90 [22.2%], p = 0.010; RR = 0.33, 95% CI 0.13-0.82). No adverse effects were observed during the study period.
No significant differences were observed in the occurrence of fasting headaches between the two groups on most days during the study period. Additional studies are required to address fasting headaches during the first week of Ramadan.
在斋月的头几天,禁食头痛经常发生,由于要禁食,因此治疗具有挑战性。
本研究旨在评估延长释放对乙酰氨基酚预防禁食头痛的效果。
一项随机、开放标签的临床试验研究了在斋月的头一周每天服用 1330 毫克延长释放对乙酰氨基酚预防禁食头痛的效果。通过沙特国王大学医学城的临床试验单位招募年龄在 18 岁及以上的成年人。符合条件的参与者在斋月的头一周每天禁食 13.5 小时。治疗组和对照组的参与者通过使用带有每日在线链接或电话的标准化头痛日记量表进行自我报告,以调查头痛症状的发生、严重程度和时间。主要结局是在斋月的头一周禁食期间头痛发作的频率。
共有 238 名参与者入组并随机分组。其中,173 名至少遵循了方案(80 名治疗,93 名对照)至少第一天,并纳入了分析。大多数参与者年轻且健康,平均年龄为 32.2±10.2 岁。研究中有更多的男性(102/173;59.0%),一小部分参与者吸烟(31/173;17.9%),几乎所有参与者都报告喝咖啡(165/173;95.4%);尽管如此,这些特征在研究中的两组之间均匀分布。第 1 天的头痛发作总发生率为 33.0%(57/173),第 7 天降至 11.3%(18/159)。平均在 7 天内,从广义估计方程模型的结果来看,治疗对头痛的发生率没有显著影响(β=-0.398,p=0.084;比值比=0.67,95%置信区间[CI]0.42-1.06)。此外,在治疗和对照组之间,头痛发作的发生率最初没有显著差异。然而,与对照组相比,治疗组在第 3 天(4/72[5.6%]vs.15/91[16.5%],p=0.031;相对风险[RR]=0.34,95%CI 0.12-0.97)和第 6 天(5/69[7.2%]vs.20/90[22.2%],p=0.010;RR=0.33,95%CI 0.13-0.82)禁食期间的头痛发作次数明显更少。在研究期间未观察到不良反应。
在研究期间的大多数日子里,两组之间禁食头痛的发生没有显著差异。需要进一步的研究来解决斋月第一周的禁食头痛问题。