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Long Covid19

Effectiveness of Testofen Compared to Placebo on Long COVID Symptoms

Sponsored by RDC Clinical Pty Ltd

About this trial

Last updated 8 months ago

Study ID

FENCOV

Status

Recruiting

Type

Interventional

Phase

Phase 3

Placebo

No

Accepting

18-75 Years
18+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 2 months ago

What is this trial about?

This is a double blind, randomised, placebo-controlled trial to evaluate orally-dosed Testofen (a specialised extract of Trigonella foenum-graecum (Fenugreek) seed) compared to placebo on post COVID-19 symptoms in otherwise healthy participants 18 years and over.

What are the participation requirements?

Yes

Inclusion Criteria

- Adults 18 years and over

- Able to provide informed consent

- Diagnosed with COVID-19 infection (RAT or PCR test) >4 weeks, but < 12 months and experiencing post COVID symptoms (1)

- Agree not to participate in another clinical trial while enrolled in this trial

1. Common post COVID symptoms may include fatigue, cough, chest pain, hair loss, weakness, joint pain, cardiac issues, neurocognitive impairment including memory loss, and decreased quality of life
No

Exclusion Criteria

- Symptoms resulting from vaccination (2)

- Unstable or serious illness (e.g., serious mood disorders, neurological disorders such as MS, kidney disease, liver disease, heart conditions, diabetes, thyroid gland dysfunction) (3)

- Current malignancy (excluding BCC) or chemotherapy and radiotherapy treatment for malignancy within the previous 2 years

- Receiving/prescribed coumandin (Warfarin), heparin, dalteaparin, enoxaparin or other anticoagulation therapy

- Receiving pharmaceutical treatment for anxiety, libido, low energy

- Active smokers, nicotine use, alcohol, or drug (prescription or illegal substances) abuse

- Chronic past and/or current alcohol use (>14 alcoholic drinks per week)

- Allergic to any of the ingredients in the active or placebo formula

- Known pregnant or lactating women

- Any condition which in the opinion of the investigator makes the participant unsuitable for inclusion

- Participants who have participated in any other related clinical study during the past 1 month

- History of infection in the month prior to the study (2) Symptoms must be as a direct result of having contracted COVID. If symptoms only appeared within 2 weeks of a vaccination it will be considered a vaccine injury and not classed as a result of COVID. (3) An unstable illness is any illness that is currently not being treated with a stable dose of medication or is fluctuating in severity. A serious illness is a condition that carries a risk of mortality, negatively impacts quality of life and daily function and/or is burdensome in symptoms and/or treatments.

Locations

Location

Status

Recruiting