SleepCited

Temazepam or Melatonin Versus Placebo for the Treatment of Insomnia in Advanced Cancer: A Three-Arm, Double-Blind, Phase III, Multicenter, Randomized Clinical Trial.

Ruwani Mendis, Aaron Wong, Simon Frenkel, Anne Marie Southcott, Chris J Selman et al.
RCT Journal of palliative medicine 2024 5 件の引用

研究デザイン

研究タイプ
RCT
サンプルサイズ
21
対象集団
Patients with advanced cancer (ISI score >11); multicenter Phase III RCT; 21 participants randomized to temazepam (n=9), melatonin prolonged release (n=8), or placebo (n=4).
介入
Temazepam or Melatonin Versus Placebo for the Treatment of Insomnia in Advanced Cancer: A Three-Arm, Double-Blind, Phase III, Multicenter, Randomized Clinical Trial. None
比較対照
Placebo
主要アウトカム
Insomnia Severity Index (ISI) score at day 8
効果の方向
Positive
バイアスリスク
Moderate

抄録

Background: Sleep disturbance has a prevalence of 30-78% in patients with advanced cancer. While pharmacotherapy is common, randomized controlled studies (RCTs) investigating available agents are limited. This study examines the efficacy and safety of temazepam or melatonin versus placebo for sleep in advanced cancer. Methods: This is a multicenter, randomized, double-blind, placebo-controlled study of temazepam, melatonin prolonged release (PR) or placebo for insomnia in patients with advanced cancer, and an insomnia severity index (ISI) score of >11. Results: Twenty-one participants were randomized: nine to temazepam, eight to melatonin, and four to placebo. Baseline characteristics between groups were similar. The adjusted mean difference in day 8 ISI score versus placebo was -9.1 (95% confidence interval [CI] -17.5, 0.7, p = 0.04) for temazepam and -9.6 (95% CI -18,-1.2, p = 0.03) for melatonin PR. There was no improvement in global quality of life. Both agents were well tolerated. Conclusion: Temazepam and melatonin PR were associated with a clinically significant improvement in patient-reported insomnia severity compared with placebo. Findings need confirmation with larger patient numbers.

要約

Temazepam and melatonin PR were associated with a clinically significant improvement in patient-reported insomnia severity compared with placebo, and both agents were well tolerated.

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