Overview
Pilot Study Into LDN and NAD+ for Treatment of Patients With Post-COVID-19 Syndrome
Status:
Recruiting
Recruiting
Trial end date:
2022-03-01
2022-03-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Pilot study into low dose naltrexone (LDN) and NAD+ for treatment of patients with post-COVID-19 syndrome.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
AgelessRxTreatments:
Naltrexone
Niacinamide
Criteria
Inclusion Criteria:- 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
Exclusion Criteria:
- 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+