Overview

Pilot Study Into LDN and NAD+ for Treatment of Patients With Post-COVID-19 Syndrome

Status:
Recruiting
Trial end date:
2022-03-01
Target enrollment:
0
Participant gender:
All
Summary
Pilot study into low dose naltrexone (LDN) and NAD+ for treatment of patients with post-COVID-19 syndrome.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
AgelessRx
Treatments:
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+