Skip to content

clinical study of Vardhamana Pippli Rasayana and WHO rehabilitation guidelines in the management of post Covid syndrome

Efficacy of Vardhamana Pippli Rasayana and WHO rehabilitation guidelines in the management of Post COVID 19 Syndrome - A Double arm Randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/031684
Enrollment
80
Registered
2021-03-03
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: A00-B99- Certain infectious and parasitic diseases Health Condition 2: B342- Coronavirus infection, unspecified Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Vardhmana Pippali: In group A, Pippali powder will be given ingradually in increasing and tapering dose for 30 days with Mrudwika Sharkara Control Intervention1: Rehabilitation program

Sponsors

Institute of Teaching and Research in Ayurveda Institute of National Importance Ministry of Ayush
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having lingering symptoms of COVID 19 after testing negative for the disease and extending beyond three weeks from the onset of a first symptom (Acute COVID 19).

Exclusion criteria

Exclusion criteria: 1. Positive SARS-CoV-2 PCR at the screening visit 2. Patients having severe symptoms of Post COVID 19 syndrome with co-morbidities requiring hospitalization 3. History of any of the following in the past 14 days: fever > 38.2 degrees Celsius; new or worsening respiratory symptoms (e.g. cough, dyspnea) 4. Patients having uncontrolled cardiac, renal, hepatic disease, malignancy, AIDS, diabetes 5. Pregnant and lactating women 6. Patients taking phenytoin, propranolol, theophylline (as Pippali has moderate interaction with the absorption of these drugs) 7. Patients having or progressive towards serious sequelae such as thromboembolic complications 8. COVID-19 patients whose acute illness required intensive care 9. SpO2 10. Age below 18 years & above 60 years

Design outcomes

Primary

MeasureTime frame
It is expected that the trial drugs will have immunomodulatory effect and thus will effective in the management Post COVID 19 SyndromeTimepoint: 4 weeks

Secondary

MeasureTime frame
The Vardhamana Pippali Rasayana will improve the quality of life in post COVID19 SyndromeTimepoint: 4 weeks

Countries

India

Contacts

Public ContactDr Mandip Goyal

ITRA, jamnagar

mandipgoyal22@gmail.com9427572306

Outcome results

None listed

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