Randomized Clinical Trial: Effects of Melatonin Supplementation on Sleep Quality in Patients with Advanced Glaucoma
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 64
- 试验地点
- 1
- 主要终点
- Effects of Melatonin Replacement on Sleep Quality of Patients with Advanced Glaucoma
研究概览
简要总结
A prospective, randomized, parallel, crossover, double-blind therapeutic clinical trial was conducted in accordance with the principles of the Resolution nº 466/12 of the National Health Council and was approved by the Ethics and Research Committee of the Federal University of São Paulo, project CEP/UNIFESP n:1023/2020, CAAE: 36946620.9.0000.5505. Written informed consent was obtained from all participants. The study was conducted at the Glaucoma Division and the Department of Psychobiology at the Federal University of São Paulo - UNIFESP/EPM and at the Laser Vision Eye Hospital - Santos/SP between May/2022 and July/2023.
详细描述
The study included 64 patients with a diagnosis of advanced primary open-angle glaucoma in both eyes.
Patients were classified as glaucoma cases if they had at least 3 repeatable, consecutive, abnormal visual field test results, defined as a pattern standard deviation (PSD) outside the 95% normal confidence limits or a Glaucoma Hemifield Test (GHT) result outside normal limits matching the appearance of the optic disc, presenting a Mean deviation of <-12.00 dB in the better eye(7,14,17), according to the Hoddap-Parish-Anderson classification for glaucoma severity, using the SITA-Standard strategy, with no involvement of the fixation region (absence of statistically significant points in the central 5º for both total and pattern deviation).
Patients were considered as glaucomatous if they had signs of glaucomatous optic neuropathy based on optic disc stereophotographs. Evidence of glaucomatous damage to the optic disc nerve was considered if they had RNFL defects or localized or diffuse neuroretinal rim loss. There were 32 participants in the melatonin group and 32 in the placebo group. The age range of the volunteers was over 40 years and under 80 years.
Subjects were excluded if they were younger than 40 or older than 80 years; best-corrected visual acuity of less than 0.4 logMAR; Patients who work at night or recently traveled across time zones, use topical or systemic medications that could disrupt circadian rhythms, for example Benzodiazepines, Non-benzodiazepines (hypnotics), Sedative antidepressants, Melatonin and melatonin agonists, patients with previously defined obstructive sleep apnea or other disorders such as depression and insomnia were excluded. Only patients with an open angle on gonioscopy were included in our study.
Each participant received melatonin 5 mg and placebo for a period of 30 days at different time points. The packages were identical, each labeled with the letters F and I. Only the supervisor Dr. Augusto Paranhos Junior, had knowledge of which package contained the original drug. Additionally, the pills within the packages were identical and supplied by the same researcher, who was not informed about the significance of the letters on the packaging.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
盲法说明
there is no
入排标准
- 年龄范围
- 40 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosis of Primary Open-Angle Glaucoma: Must have a confirmed diagnosis of primary open-angle glaucoma.
- •Cup-to-Disc Ratio > 0.6: The ratio of cup to disc on optic disc imaging must be greater than 0.
- •Visual Acuity ≥ 0.4 logMAR: Participants must have a visual acuity of 0.4 logMAR or better in the better eye.
- •Age: Participants must be aged 40 to 80 years, inclusive.
排除标准
- •Pregnancy: Female participants who are pregnant or planning to become pregnant during the study period.
- •Current or Past Diagnosis of Depression: Participants with a current or past history of depression.
- •Corneal or Retinal Diseases: History or active disease of the cornea or retina (e.g., diabetic retinopathy, macular degeneration).
- •Shift Work: Participants who work night shifts or irregular hours.
- •Travel Across Time Zones: Participants who have traveled across time zones in the last 30 days prior to enrollment.
- •Diagnosed Obstructive Sleep Apnea: History of obstructive sleep apnea or a current diagnosis of the condition.
研究组 & 干预措施
melatonin treatment group
Each participant received melatonin 5 mg and placebo for a period of 30 days
干预措施: Experimental: melatonin treatment group (Drug)
melatonin treatment group
Each participant received melatonin 5 mg and placebo for a period of 30 days
干预措施: Placebo comparator: placebo treatment group (Drug)
placebo treatment group
Each participant received melatonin 5 mg and placebo for a period of 30 days
干预措施: Experimental: melatonin treatment group (Drug)
placebo treatment group
Each participant received melatonin 5 mg and placebo for a period of 30 days
干预措施: Placebo comparator: placebo treatment group (Drug)
结局指标
主要结局
Effects of Melatonin Replacement on Sleep Quality of Patients with Advanced Glaucoma
时间窗: From enrollment to the end of treatment in 2 months
To compare the quality of sleep in patients with advanced glaucoma after 30 days of melatonin 5 mg and 30 days of placebo. The comparison of efficacy between groups will be assessed based on the improvement in sleep quality between medications.
次要结局
- Effects of Melatonin Replacement on Sleep Quality of Patients with Advanced Glaucoma(From registration to the end of treatment in 2 months)
研究者
Priscilla Fernandes Nogueira
Principal Investigator
University of Sao Paulo
