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Sahadevi Choorna for COVID 19

Evaluation of Effect of Sahadevi (Vernonia cinerea) Powder in symptomatic improvement of mild to moderate COVID 19 Positive Patients a double blind placebo controlled study.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026575
Enrollment
48
Registered
2020-07-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere Health Condition 2: J969- Respiratory failure, unspecified

Interventions

Intervention1: Cap of Sahadevi Powder: Dose 2 cap[1gm powder] Frequency Thrice daily with warm water after food route of administration oral Duration of therapy 15 days Control Intervention1: Cap pla

Sponsors

Parul Institute of Ayurved Parul University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Confirmed cases of COVID 19 infections within three days of diagnosis and showing mild to moderate symptoms Subjects who are not suffering from any comorbid condition of COVID 19 diabetes hypertension IHD Subjects willing to sign informed consent

Exclusion criteria

Exclusion criteria: Subjects who are known cases of immunecompromised or autoimmune condition such as HIV Pregnant and lactating women Patients needing intensive care unit treatment protocol

Design outcomes

Primary

MeasureTime frame
Reduction in symptom of COVID 19 To reduce Complication of diseaseTimepoint: 3rd day 5th day 8th day 16th day after intervention

Secondary

MeasureTime frame
Improvement in Quality of life of patients effect on routine investigation after starting the trialTimepoint: 3rd day 5th day 8th day 16th day after intervention

Countries

India

Contacts

Public ContactDr Nandakishor P Umale

Parul Institute of Ayurveda and Research Parul University

nandkishor.umale260079@paruluniversity.ac.in8379815979

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026