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Evaluation of the effect of plant compounds extract (including aqueous extract of Ador-Cancer, saffron petals and mountain tea) in patients with coronary disease

Evaluation of the effects of the aqueous extract of Alhagi papilionaceae or petals Saffron petal and mountain tea herbs on the clinical and paraclinical symptoms of COVID-19 patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211108053002N1
Enrollment
40
Registered
2021-11-21
Start date
2021-12-22
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

symptoms of COVID-19 patients. COVID-19, virus identified

Interventions

Intervention 1: Intervention group: Patients with Covid-19 will consume 10 ml of syrup containing aqueous extracts of Ador-Cancer, saffron petals and mountain tea 3 times a day. In this study, no spec

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria in this study include all patients who have been diagnosed with Covid 19 infection and do not have other infections or diseases such as influenza, pulmonary insufficiency, ARDS pneumonia and other cold symptoms, as well as files with complete data. Consciously taken from patients.

Exclusion criteria

Exclusion criteria: Exclusion criteria included patients who had other infections or diseases such as influenza, pulmonary insufficiency, ARDS pneumonia and other cold symptoms and the result of Qovid 19 infection is negative. Also, files with incomplete data will be removed from this study. Obviously, conscious dissatisfaction also leads to exclusion from the study. Patients who were hospitalized and their clinical condition was deteriorating were excluded from the study and lung CT scans were obtained from patients. Patients with oxygen levels less than 93 mm Hg were excluded from the study

Design outcomes

Primary

MeasureTime frame
The length of hospitalization of patients with Covid-19. Timepoint: 21 days after starting of intervention. Method of measurement: By referring to the patient's medical record.;The mortality in patients with Covid-19. Timepoint: 21 days after starting of intervention. Method of measurement: By referring to the patient's medical record.;The pulmonary infiltration in patients with Covid-19. Timepoint: 7, 14 and 21 days after starting of intervention. Method of measurement: With CT scan.

Secondary

MeasureTime frame
Side effects from the use of herbal compounds (COVID-herbs). Timepoint: 7, 14 and 21 days after starting of intervention. Method of measurement: Refer to the medical file and complete a special questionnaire for complications.;The liver function in patients with Covid-19. Timepoint: 7, 14 and 21 days after starting of intervention. Method of measurement: Evaluation of SGOT and SGPT enzymes using ELISA kit.;The kidney function in patients with Covid-19. Timepoint: 7, 14 and 21 days after starting of intervention. Method of measurement: Evaluation of chemical parameters such as BUN and Creatinine by colorimetric method with autoanalyzer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Drehkordi

Rafsanjan University of Medical Sciences

mojgan.noroozi@yahoo.com+98 913 290 6232

Outcome results

None listed

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