NCT06489860

Brief Summary

SARS-CoV-2 produced strong pluripotent stem cells and brain cells to protect Telomere chromosomes to maintain Acid Deoxyribonucleic (ADN) Molecules.

Trial Health

15
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Jan 2025

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 5, 2024

Completed
4 months until next milestone

First Posted

Study publicly available on registry

July 8, 2024

Completed
7 months until next milestone

Study Start

First participant enrolled

January 28, 2025

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 30, 2025

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 4, 2025

Completed
Last Updated

September 4, 2025

Status Verified

August 1, 2025

Enrollment Period

2 days

First QC Date

March 5, 2024

Last Update Submit

August 24, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • SARS-CoV-2

    1. Parameters: Humidification, Unit: %, Result: 4.40, Test Method: ISO 7932: 2004. 2. Cadmium (Cd), mg/Kg, 0.1, CASE.TN.0018 (Ref. AOAC 999.11). 3. Hydrargyrum (Hg), mg/Kg, 0.01, CASE.TN.0141 (Ref . EPA Method 7473). 4. Plumbum (Pb), mg/liter, 0.001, SMEWW3030E 2017: 31258: 2017. 5. Cadmium (Cd), mg/liter, 0.0001, SMEWW3030E 2017: 31258: 2017. . 6. Arsen (As), mg/liter, 0.001, SMEWW3030E 2017: 31258: 2017. 7. Hydrargyrum (Hg), mg/liter, 0.0001, SMEWW3030E 2017: 31258: 2017. 8. Clostridium perfringents, CFU/g, \< 10, ISO 7937:2004. 9. Coliforms, CFU/g, \< 10, ISO 4832:2006 (\*). 10. Escherichia coli, CFU/g, \< 10, ISO 7937:2006. 11. Salmonella, /25g, Not detected, ISO 7937:2007. 12. Staphylococcus aureus, CFU/g, \< 10, ISO 7937:2008. 13. Total Yeasts molds, CFU/g, \< 10, ISO 7937:2009. 14. Total Aerobic Microbial, CFU/g, 1.0 x 100, ISO 7937:2010. 15. Vibrio parahaemolyticuc, /25g, Not detected, ISO 7937:2011. .

    From September to October, 2024

Study Arms (1)

SARS-CoV-2 Safety Study for the Treatment of COVID-19

EXPERIMENTAL

Directions: For adults and for Children 1-12 years old. Indication:SARS-CoV-2 Ingredients: Organic Rice 95% and Honey 5% Powder (whole) 1g. Mix one packet with 6.8 fl oz (200 ml) of hot water (220ºF/100ºC) about three minutes until dissolved. Participants: Use 4 to 5 packets, use one pack each time after two hours. Humidification: \<5% Dosage Form: Powder form Dosage Strength: 1.0 G/ 1 Unit, use one pack of 1 g for each time Use within two years from the manufacturing date. Storage normal conditions in dry, cool and temperature from 15 °C to 32 °C Store in a dry environment (75% humidity).

Drug: HIVDrug: Malignant Neoplasms Safety Study for the Treatment of Neoplasms

Interventions

HIVDRUG

Directions: For adults and for Children 1-12 years old. Indication: HIV Ingredient: Organic Rice 93% and Honey 7% Powder (whole) 1g. Masking: None (Open Label) Mix one packet with 6.8 fl oz (200 ml) of hot water (220ºF/100ºC) about three minutes until dissolved. Participants: Use 4 to 5 packets, use one pack each time after two hours. Humidification: \<5% Dosage Form: Powder form Dosage Strength: 1.0 G/ 1 Unit, use one pack of 1 g for each time Use within two years from the manufacturing date

Also known as: HIV Safety Study for the Treatment of Anti-AIDS Drug
SARS-CoV-2 Safety Study for the Treatment of COVID-19

Directions: For adults and for Children 1-12 years old. Indication: Malignant Neoplasms . Ingredient: Organic Rice 92% and Honey 8% Powder (whole) 1g. Mix one packet with 6.8 fl oz (200 ml) of hot water (220ºF/100ºC) about three minutes until dissolved. Participants: Use 4 to 5 packets, use one pack each time after two hours. Humidification: \<5% Dosage Form: Powder form Dosage Strength: 1.0 G/ 1 Unit, use one pack of 1 g for each time Use within two years from the manufacturing date.

Also known as: Malignant Neoplasms
SARS-CoV-2 Safety Study for the Treatment of COVID-19

Eligibility Criteria

Age1 Year - 130 Years
Sexall(Gender-based eligibility)
Gender Eligibility DetailsDirections: For adults and for Children 1-12 years old.
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • SARS-CoV-2

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Zarin DA, Tse T, Williams RJ, Califf RM, Ide NC. The ClinicalTrials.gov results database--update and key issues. N Engl J Med. 2011 Mar 3;364(9):852-60. doi: 10.1056/NEJMsa1012065.

Related Links

Study Officials

  • PHUOC T DO

    DHA Coffee Co., Ltd

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
phase 2
Allocation
NA
Masking
NONE
Masking Details
Directions: For adults and for Children 1-12 years old. Indication: SARS-CoV-2 Ingredient: Organic Rice 95% and Honey 5% Powder (whole) 1g. Mix one packet with 6.8 fl oz (200 ml) of hot water (220ºF/100ºC) about three minutes until dissolved. Participants: Use 4 to 5 packets, use one pack each time after two hours. Humidification: \<5% Dosage Form: Powder form Dosage Strength: 1.0 G/ 1 Unit, use one pack of 1 g for each time Use within two years from the manufacturing date. Storage normal conditions in dry, cool and temperature from 15 °C to 32 °C Store in a dry environment (75% humidity).
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: SARS-CoV-2. Directions: For adults and for Children 1-12 years old. Indication: SARS-CoV-2. Ingredient: Organic Rice 95% and Honey 5% Powder (whole) 1g.
Sponsor Type
INDUSTRY
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
DHA Coffee Co., Ltd

Study Record Dates

First Submitted

March 5, 2024

First Posted

July 8, 2024

Study Start

January 28, 2025

Primary Completion

January 30, 2025

Study Completion

February 4, 2025

Last Updated

September 4, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

20 -1 g Packets Net Weight 0.70 oz (20 g) Directions: For adults and for Children 1-12 years old. Indication: Treated the SARS-CoV-2 treatment COVID-19 within 20 days Ingredient: Organic Rice 95% and Honey 5% Powder (whole) 1g. Mix one packet with 6.8 fl oz (200 ml) of hot water (220ºF/100ºC) about three minutes until dissolved. Participants: Use 4 to 5 packets, use one pack each time after two hours. Use within two years from the manufacturing date. Humidification: \<5% Dosage Form: Powder form Dosage Strength: 1.0 G/ 1 Unit, use one pack of 1 g for each time Storage normal conditions in dry, cool and temperature from 15 °C to 32 °C Store in a dry environment (75% humidity).