Honey and Nigella sativa against COVID‐19 in Pakistan (HNS‐COVID‐PK): A multicenter placebo‐controlled randomized clinical trial

Until now, no specific and effective treatment exists for coronavirus disease 2019 (COVID‐19). Since honey and Nigella sativa (HNS) have established antiviral, antibacterial, antiinflammatory, antioxidant, and immunomodulatory properties, we tested their efficacy for this disease in a multicenter, p...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Phytotherapy research 2023-02, Vol.37 (2), p.627-644
Hauptverfasser: Ashraf, Sohaib, Ashraf, Shoaib, Ashraf, Moneeb, Imran, Muhammad Ahmad, Kalsoom, Larab, Siddiqui, Uzma N., Farooq, Iqra, Akmal, Rutaba, Akram, Muhammad Kiwan, Ashraf, Sidra, Ghufran, Muhammad, Majeed, Nighat, Habib, Zaighum, Rafique, Sundas, ‐Abdin, Zain‐ul, Arshad, Shahroze, Shahab, Muhammad Sarmad, Ahmad, Sohail, Zheng, Hui, Mirza, Ali Rafique, Zulfiqar, Sibgha, Anwar, Muhamad Imran, Humayun, Ayesha, Mahmud, Talha, Saboor, Qazi Abdul, Ahmad, Ali, Ashraf, Muhammad, Izhar, Mateen
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Until now, no specific and effective treatment exists for coronavirus disease 2019 (COVID‐19). Since honey and Nigella sativa (HNS) have established antiviral, antibacterial, antiinflammatory, antioxidant, and immunomodulatory properties, we tested their efficacy for this disease in a multicenter, placebo‐controlled, and randomized clinical trial at four medical care facilities in Pakistan. RT‐PCR confirmed COVID‐19 adults showing moderate or severe disease were enrolled in the trial. Patients were randomly assigned in a 1:1 ratio to receive either honey (1 g kg−1 day−1) and Nigella sativa seeds (80 mg kg−1 day−1) or a placebo for up to 13 days along with standard care. The outcomes included symptoms' alleviation, viral clearance, and 30‐day mortality in the intention‐to‐treat population. Three hundred and thirteen patients, 210 with moderate and 103 with severe disease, underwent randomization from April 30 to July 29, 2020. Among the moderate cases, 107 were assigned to HNS, whereas 103 were assigned to the placebo group. Among the severe cases, 50 were given HNS, and 53 were given the placebo. HNS resulted in ~50% reduction in time taken to alleviate symptoms as compared to placebo (moderate cases: 4 vs. 7 days, Hazard Ratio [HR]: 6.11; 95% Confidence Interval [CI]: 4.23–8.84, p 
ISSN:0951-418X
1099-1573
DOI:10.1002/ptr.7640