Pilot Study Into LDN and NAD+ for Treatment of Patients With Post-COVID-19 Syndrome
Completed · Phase 2
Conditions studied: Covid19, Long COVID-19, Post-COVID-19 Syndrome
In brief
Pilot study into low dose naltrexone (LDN) and NAD+ for treatment of patients with post-COVID-19 syndrome.
Key facts
- Study ID
- NCT04604704
- Run by
- AgelessRx
- People needed
- 36
- Starts
- 2021-01-28
- Expected to finish
- 2023-01-23
- Last updated by the study team
- 2023-01-25
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Any ethnicity
- Adequate cognitive function to be able to give informed consent
- Technologically competent to complete web forms and perform video calls with the PI
- Positive PCR test (polymerase chain reaction) result for SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) 1-4 months before enrollment
- A fatigue score above 9 in the Chalder Fatigue scale upon enrollment
- Willing to fill out regular questionnaires
- Willing to use LDN and NAD patches
You may not qualify if…
- Clinically significant kidney, heart, Hepatic impairment as determined by clinical judgement
- Taking opioid analgesics, or undergoing treatment for opioid addiction
- Opioid dependence or withdrawal syndrome
- Known sensitivity to naltrexone
- Suspected or confirmed pregnancy or breastfeeding
- Known issues with using iontophoresis patches
- Active cancers
- Enrolled in another trial
- Current users of LDN or NAD+
Where it is running
- AgelessRx — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
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