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The Efficacy of Nigella Sativa Versus VitaminD3 as Supplement Therapy in Coronavirus Disease 2019 (COVID-19) (COVID-19)

Primary Purpose

Covid19

Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Nigella Sativa capsule twice daily
Sponsored by
Ain Shams University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with mild-moderate COVID-19 according to the classification (Table 1)
  2. Adult (18 - 65 years old).
  3. Polymerase chain reaction (PCR)-confirmed infection with Severe Acute Respiratory Syndrome Coronavirus-2.

Exclusion Criteria:

  1. Patients with severe illness requiring admission to intensive care unit.
  2. Asymptomatic patients.
  3. Severe chronic kidney disease (i.e. estimated glomerular filtration rate < 30 mL/min) or end stage renal disease requiring dialysis
  4. Severe chronic liver disease (Alanine transaminase or Aspartate transaminase > 5 times the upper limit of normal).
  5. contraindications to any of the interventional drugs.
  6. Pregnancy or breast feeding.
  7. Allergy to any of the interventional.

Sites / Locations

  • Respiratory System specialized hospital at Kobry Elobba Military Medical hospitals.Recruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

No Intervention

Active Comparator

Active Comparator

Active Comparator

Arm Label

group 1

group 2

group 3

group 4

Arm Description

Twenty five patients will be administered only the standard treatment regimen according to Ministry Of Health, and Population management protocol for COVID-19 patients (November 2020).

Twenty five patients will be administered a single dose (900mg) of Nigella Sativa capsule twice daily plus standard therapy

Twenty five patients will be administered a single dose (2000 IU) of vitamin D3 tablet once daily plus standard therapy

Twenty five patients will be administered a single dose (900 mg) of Nigella Sativa capsule twice daily, and single dose of vitamin D3 tablet (2000 IU) once daily plus standard therapy.

Outcomes

Primary Outcome Measures

The safety and efficacy of Nigella Sativa and Vitamin D3 as a supplement for management of COVID-19 will be evaluated and recorded.
The patient will be examined by the physician and the rate of occurrence of any of the following signs and symptoms on the participants will be reported: Fever -Runny nose - Red swollen eyes Fatigue - Shortening in breath - Skin rash Cough - Body aches Sore throat - Diarrhea, and/or Vomiting Headache - Loss of taste and/or Smell
Assessment of patient health status before and after treatment intervention for a period of 14 days will be done
All patients will be evaluated during the study period (14 days) by undergoing PCR test after two days from absence of any clinical presentation, Then if the PCR is negative, the patient will be discharged from the hospital and complete his medication course at home. If the result is positive then the patient will undergo another PCR testing on day 14 with no further follow up .

Secondary Outcome Measures

The recovery rate of patients, Intensive care unit admission rate of patients and the Length of hospital stay of the patients will be recorded
Length of hospital stay and number of patients need ICU admission due to deterioration of cases and progression of disease.
The following laboratory testing will be performed at least twice during the study period:
C-Reactive Protein in mg/L. Arterial Blood Gases[carbon dioxide partial pressure, oxygen partial pressure] in mm Hg. Kidney function [serum creatinine, blood urea nitrogen ] in mg/dL. liver function [ Alanine aminotransferase, Aspartate aminotransferase] in IU/L . Erythrocyte sedimentation rate in mm/hr. Complete blood picture. Serum Ferritin in ug/L international normalized ratio, prothrombin time, partial thromboplastin time in seconds Polymerase chain reaction (PCR). Computed tomography (CT) chest . Length of hospital stay and number of patients need ICU admission due to deterioration of cases and progression of disease.

Full Information

First Posted
July 9, 2021
Last Updated
July 27, 2021
Sponsor
Ain Shams University
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1. Study Identification

Unique Protocol Identification Number
NCT04981743
Brief Title
The Efficacy of Nigella Sativa Versus VitaminD3 as Supplement Therapy in Coronavirus Disease 2019 (COVID-19)
Acronym
COVID-19
Official Title
Evaluation of The Efficacy of Nigella Sativa Versus VitaminD3 as Supplement Therapy in Management of Coronavirus Disease 2019 (COVID-19)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 21, 2021 (Anticipated)
Primary Completion Date
September 30, 2021 (Anticipated)
Study Completion Date
December 30, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ain Shams University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The aim this study is to investigate the safety and efficacy of Nigella Sativa versus Vitamin D3 versus Nigella Sativa / vitamin D3 combination as supplement for management of COVID-19 .
Detailed Description
Corona-virus disease-19 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2, and this virus was first originated from Wuhan city of Hubei province of China spreading around the globe. The prominent symptoms of COVID-19 include fever, cough, dyspnea, and other symptoms noted in patients affected by COVID-19 that includes; chills, repeated shaking with chills, muscle pain, headache, sore throat, and new loss of taste or smell. In addition, the emergency warning signs of COVID-19 include difficulty breathing or shortness of breath, persistent pain or pressure in the chest, new confusion or inability to arouse and bluish lips or face and the patients experiencing any of these signs should get immediate medical attention. Herbal medicines are used by many people to try to improve their health upon the believe that "natural products" are always safe, and good for immunity based on the traditional knowledge .There is a potential of Nigella Sativa to treat the patients with COVID-19. Nigella Sativa (NS), a widely used medicinal plant of the family Ranunculaceae ; commonly known as Black Cumin, has been shown to exert antiviral effects against a variety of viruses such as Mouse Cytomegalovirus and Hepatitis C Virus (HCV) . The components' antimicrobial properties against various microbes as well as their anti-inflammatory and immuno-modulatory effects have also been established . The immune system defends the body from foreign, invading organisms, promoting protective immunity, while maintaining tolerance to self. The implications of vitamin deficiency on the immune system have become clearer in recent years, and in the context of vitamin D deficiency, the increased susceptibility to infection observed, especially in a genetically susceptible host to autoimmunity. The classical actions of vitamin D are to promote calcium homeostasis, and to promote bone health. In humans, vitamin D is obtained from the diet, or synthesized in the skin as vitamin D is cutaneously produced after exposure to UV light, its synthesis is influenced by latitude, season, use of sun-block and skin pigmentation. Melanin absorbs UV radiation inhibiting the synthesis of vitamin D from 7-dihydrocholesterol. This initial vitamin D compound is inactive form; hydroxylation in the liver to form the active 25 hydroxy vitamin D3 (25 D). Vitamin D is the most reliable measurement of an individual's vitamin D status. It is converted in the kidney to the active compound 1,25 dihydroxy vitamin D (1,25 D) or calcidiol by 1-α-hydroxylase (CYP27B1), an enzyme which is stimulated by parathormone. A principal defense against uncontrolled inflammation, and against viral infection in general, is provided by T regulatory lymphocytes (Tregs). Treg levels have been reported to be low in many COVID-19 patients, and can be increased by vitamin D supplementation. Low vitamin D levels have been associated with an increase in inflammatory cytokines, and a significantly increased risk of pneumonia, and viral upper respiratory tract infections.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Controlled Parallel Open label Randomized Clinical Trial .
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
group 1
Arm Type
No Intervention
Arm Description
Twenty five patients will be administered only the standard treatment regimen according to Ministry Of Health, and Population management protocol for COVID-19 patients (November 2020).
Arm Title
group 2
Arm Type
Active Comparator
Arm Description
Twenty five patients will be administered a single dose (900mg) of Nigella Sativa capsule twice daily plus standard therapy
Arm Title
group 3
Arm Type
Active Comparator
Arm Description
Twenty five patients will be administered a single dose (2000 IU) of vitamin D3 tablet once daily plus standard therapy
Arm Title
group 4
Arm Type
Active Comparator
Arm Description
Twenty five patients will be administered a single dose (900 mg) of Nigella Sativa capsule twice daily, and single dose of vitamin D3 tablet (2000 IU) once daily plus standard therapy.
Intervention Type
Dietary Supplement
Intervention Name(s)
Nigella Sativa capsule twice daily
Other Intervention Name(s)
single dose of vitamin D3 tablet (2000 IU) once daily
Intervention Description
investigate the safety and efficacy of Nigella Sativa versus Vitamin D3 versus Nigella Sativa / vitamin D3 combination as supplement for management of COVID-19 .
Primary Outcome Measure Information:
Title
The safety and efficacy of Nigella Sativa and Vitamin D3 as a supplement for management of COVID-19 will be evaluated and recorded.
Description
The patient will be examined by the physician and the rate of occurrence of any of the following signs and symptoms on the participants will be reported: Fever -Runny nose - Red swollen eyes Fatigue - Shortening in breath - Skin rash Cough - Body aches Sore throat - Diarrhea, and/or Vomiting Headache - Loss of taste and/or Smell
Time Frame
baseline and 14 days
Title
Assessment of patient health status before and after treatment intervention for a period of 14 days will be done
Description
All patients will be evaluated during the study period (14 days) by undergoing PCR test after two days from absence of any clinical presentation, Then if the PCR is negative, the patient will be discharged from the hospital and complete his medication course at home. If the result is positive then the patient will undergo another PCR testing on day 14 with no further follow up .
Time Frame
baseline and 14 days
Secondary Outcome Measure Information:
Title
The recovery rate of patients, Intensive care unit admission rate of patients and the Length of hospital stay of the patients will be recorded
Description
Length of hospital stay and number of patients need ICU admission due to deterioration of cases and progression of disease.
Time Frame
14 days
Title
The following laboratory testing will be performed at least twice during the study period:
Description
C-Reactive Protein in mg/L. Arterial Blood Gases[carbon dioxide partial pressure, oxygen partial pressure] in mm Hg. Kidney function [serum creatinine, blood urea nitrogen ] in mg/dL. liver function [ Alanine aminotransferase, Aspartate aminotransferase] in IU/L . Erythrocyte sedimentation rate in mm/hr. Complete blood picture. Serum Ferritin in ug/L international normalized ratio, prothrombin time, partial thromboplastin time in seconds Polymerase chain reaction (PCR). Computed tomography (CT) chest . Length of hospital stay and number of patients need ICU admission due to deterioration of cases and progression of disease.
Time Frame
14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with mild-moderate COVID-19 according to the classification (Table 1) Adult (18 - 65 years old). Polymerase chain reaction (PCR)-confirmed infection with Severe Acute Respiratory Syndrome Coronavirus-2. Exclusion Criteria: Patients with severe illness requiring admission to intensive care unit. Asymptomatic patients. Severe chronic kidney disease (i.e. estimated glomerular filtration rate < 30 mL/min) or end stage renal disease requiring dialysis Severe chronic liver disease (Alanine transaminase or Aspartate transaminase > 5 times the upper limit of normal). contraindications to any of the interventional drugs. Pregnancy or breast feeding. Allergy to any of the interventional.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amal A Elkholy
Phone
+201060355448
Email
amalanas9@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Shimaa A. Aly, Master
Phone
+201223844103
Email
shimaa.aly90@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nagwa A. Sabri, professor
Organizational Affiliation
Department of Clinical Pharmacy
Official's Role
Study Chair
Facility Information:
Facility Name
Respiratory System specialized hospital at Kobry Elobba Military Medical hospitals.
City
Cairo
ZIP/Postal Code
012345
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
shimaa A. Aly, master
Phone
+201223844103
Email
shimaa.aly90@gmail.com
First Name & Middle Initial & Last Name & Degree
Osama S. Beskales, Ass. Prof.
Phone
+201223844103
Email
shimaa.aly90@gmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
31986264
Citation
Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, Zhang L, Fan G, Xu J, Gu X, Cheng Z, Yu T, Xia J, Wei Y, Wu W, Xie X, Yin W, Li H, Liu M, Xiao Y, Gao H, Guo L, Xie J, Wang G, Jiang R, Gao Z, Jin Q, Wang J, Cao B. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020 Feb 15;395(10223):497-506. doi: 10.1016/S0140-6736(20)30183-5. Epub 2020 Jan 24. Erratum In: Lancet. 2020 Jan 30;:
Results Reference
background
PubMed Identifier
32179124
Citation
Rodriguez-Morales AJ, Cardona-Ospina JA, Gutierrez-Ocampo E, Villamizar-Pena R, Holguin-Rivera Y, Escalera-Antezana JP, Alvarado-Arnez LE, Bonilla-Aldana DK, Franco-Paredes C, Henao-Martinez AF, Paniz-Mondolfi A, Lagos-Grisales GJ, Ramirez-Vallejo E, Suarez JA, Zambrano LI, Villamil-Gomez WE, Balbin-Ramon GJ, Rabaan AA, Harapan H, Dhama K, Nishiura H, Kataoka H, Ahmad T, Sah R; Latin American Network of Coronavirus Disease 2019-COVID-19 Research (LANCOVID-19). Electronic address: https://www.lancovid.org. Clinical, laboratory and imaging features of COVID-19: A systematic review and meta-analysis. Travel Med Infect Dis. 2020 Mar-Apr;34:101623. doi: 10.1016/j.tmaid.2020.101623. Epub 2020 Mar 13.
Results Reference
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PubMed Identifier
32322478
Citation
Horowitz RI, Freeman PR, Bruzzese J. Efficacy of glutathione therapy in relieving dyspnea associated with COVID-19 pneumonia: A report of 2 cases. Respir Med Case Rep. 2020 Apr 21;30:101063. doi: 10.1016/j.rmcr.2020.101063. eCollection 2020.
Results Reference
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PubMed Identifier
32269670
Citation
Montero-Odasso M, Goens SD, Kamkar N, Lam R, Madden K, Molnar F, Speechley M, Stranges S. Canadian Geriatrics Society COVID-19 Recommendations for Older Adults. What Do Older Adults Need To Know? Can Geriatr J. 2020 Mar 1;23(1):149-151. doi: 10.5770/cgj.23.443. eCollection 2020 Mar. No abstract available.
Results Reference
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The Efficacy of Nigella Sativa Versus VitaminD3 as Supplement Therapy in Coronavirus Disease 2019 (COVID-19)

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