Skip to content

Effect of Terminalia chebula, Pistacia lentiscus and brown sugar oral combination in covid-19 treatment

Evaluating the effect of Terminalia chebula, Pistacia lenticus and brown sugar oral preparation onrespiratory clinical findings and inflammatory indicators in patients with COVID-19

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210803052060N1
Enrollment
200
Registered
2021-09-12
Start date
2021-08-11
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

new Corona virus disease 2019. new Corona virus disease 2019

Interventions

Intervention 1: Intervention group: COVID-19 standard treatment based on the protocol recommended by the Ministry of Health for hospitalized patients (remdesivir, prophylactic anticoagulant, and low

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Men and women above 18 years with positive PCR test for Covid-19 At least two of these findings: GGO>10%, SO220, at least one underlying disease (COPD, HF, HTN, DM, Asthma, Immunodeficiency) Conscious written consent to participate in the study

Exclusion criteria

Exclusion criteria: Covid vaccination history Participation in another clinical trial

Design outcomes

Primary

MeasureTime frame
ICU admision or intubation. Timepoint: During hospitalization, daily. Method of measurement: Evaluator report.

Secondary

MeasureTime frame
Clinical symptoms(The degree of shortness of breath, cough intensity). Timepoint: During hospitalization, daily. Method of measurement: Symptoms by asking the patient as a scale indicator and signs by monitoring the patient by the assessor.;Inflammatory markers (ESR, CRP, LDH, WBC). Timepoint: before and after the 5 days intervention. Method of measurement: Quantitative laboratory measurements of blood samples.;Clinical examinations (RR, SO2). Timepoint: During hospitalization, daily. Method of measurement: Through clinical examination and use of pulse oximeter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSajjad Panahi

Artesh University of Medical Sciences

s.panahi777@yahoo.com+98 21 8609 6350

Outcome results

None listed

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