Abstract
Background:
Long covid is a debilitating chronic condition, and the effect of low dose naltrexone (LDN) on its symptoms is unclear. We aimed to determine the effectiveness of LDN on symptoms of long covid.
Methods:
We searched PubMed, Embase, and Cochrane Library for published studies; ClinicalTrials.gov and World Health Organization International Clinical Trials Registry Platform for registered ongoing studies from inception to 1 May 2025. Eligible studies were randomised controlled trials or pre-post studies in patients with long covid reporting on fatigue, quality of life, cognition, or other symptoms. Risk of bias was assessed by Newcastle-Ottawa scale.
Results:
Of 226 titles and abstracts screened, no randomised controlled trials were identified. Four observational pre-post studies from USA and Ireland (n=155) met inclusion criteria. LDN doses varied from 1mg/d to 6 mg/d. Pooled analyses showed moderate effects for reducing fatigue (Hedges’ g= -0.74; 95% CI [-1.11, -0.37]; p<0.001), brain fog (Hedges’ g= - 0.53; 95%CI [-1.01, -0.05]; p=0.03), and improving sleep quality (Hedges’ g= -0.60; 95%CI [-0.91, -0.30]; p=0.0001), and large effects for pain (Hedges’ g= -0.93; 95%CI [-1.29, -0.57]; p<0.001) and daily functioning (Hedges’ g= -0.93; 95%CI [-1.29, -0.57]; p<0.0001) in favour of LDN. Heterogeneity ranged from 0% to 62%. Risk of bias was assessed as low in all four studies. No serious adverse events were reported in the two studies that assessed safety.
Conclusion:
Limited evidence from small pre-post studies suggests LDN may improve fatigue, cognition, sleep, pain, and functioning in long covid. However, certainty of evidence is low. Well-powered trials are urgently needed to confirm efficacy, determine dosing and duration, and identify subgroups most likely to benefit.
Long covid is a debilitating chronic condition, and the effect of low dose naltrexone (LDN) on its symptoms is unclear. We aimed to determine the effectiveness of LDN on symptoms of long covid.
Methods:
We searched PubMed, Embase, and Cochrane Library for published studies; ClinicalTrials.gov and World Health Organization International Clinical Trials Registry Platform for registered ongoing studies from inception to 1 May 2025. Eligible studies were randomised controlled trials or pre-post studies in patients with long covid reporting on fatigue, quality of life, cognition, or other symptoms. Risk of bias was assessed by Newcastle-Ottawa scale.
Results:
Of 226 titles and abstracts screened, no randomised controlled trials were identified. Four observational pre-post studies from USA and Ireland (n=155) met inclusion criteria. LDN doses varied from 1mg/d to 6 mg/d. Pooled analyses showed moderate effects for reducing fatigue (Hedges’ g= -0.74; 95% CI [-1.11, -0.37]; p<0.001), brain fog (Hedges’ g= - 0.53; 95%CI [-1.01, -0.05]; p=0.03), and improving sleep quality (Hedges’ g= -0.60; 95%CI [-0.91, -0.30]; p=0.0001), and large effects for pain (Hedges’ g= -0.93; 95%CI [-1.29, -0.57]; p<0.001) and daily functioning (Hedges’ g= -0.93; 95%CI [-1.29, -0.57]; p<0.0001) in favour of LDN. Heterogeneity ranged from 0% to 62%. Risk of bias was assessed as low in all four studies. No serious adverse events were reported in the two studies that assessed safety.
Conclusion:
Limited evidence from small pre-post studies suggests LDN may improve fatigue, cognition, sleep, pain, and functioning in long covid. However, certainty of evidence is low. Well-powered trials are urgently needed to confirm efficacy, determine dosing and duration, and identify subgroups most likely to benefit.
| Original language | English |
|---|---|
| Publisher | medRxiv: the preprint server for health sciences |
| Number of pages | 15 |
| DOIs | |
| Publication status | Published - 10 Sept 2025 |