Evaluation of the effectiveness of black halilah and fennel powder in clinical symptoms of patients with coronavirus.

Phase 2

Recruiting

• Conditions: Covid19.; Covid19; U07.1

• Registration Number: IRCT20150819023685N3
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 August 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

Inpatients diagnosed with Covid 19.
Patients with Covid 19 who wish to participate in the study
No serious heart disease, liver, kidney, blood pressure above 160 mm Hg
Patients who do not receive insulin
Non-pregnancy in women.
A maximum of 72 hours have passed since the beginning of the patient's hospitalization.

Exclusion Criteria

1. Dissatisfaction with continuing treatment.
2. Need to receive medical services in the intensive care unit.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Days of hospitalization. Timepoint: Daily. Method of measurement: View patient records.;Clinical signs. Timepoint: Before treatment and 2, 4, 7 days of treatment. Method of measurement: The severity of each of the patient's clinical symptoms is measured based on the visual analog scale in patients.;Vital Signs. Timepoint: During hospitalization on a daily basis. Method of measurement: Monitoring device.

Secondary Outcome Measures

Name	Time	Method
Mortality. Timepoint: Daily patient follow-up. Method of measurement: View patient records.