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Individualized homeopathic medicine efficacy and safety in Covid-19 epidemic

Clinical trial of individualized homeopathic medicine in Covid-19 epidemic treatment and prevention: efficacy and safety evaluation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-48fd64k
Enrollment
Unknown
Registered
2021-10-28
Start date
2021-09-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

COVID-19

Interventions

Clinical Study, Randomized, Triple blind, Placebo-Controlled Intervention group: 25 adult individuals hospitalized due to Covid-19, of both sexes, will receive Bryonia alba in 30 CH, 200 CH and 1000
HP4.018.158.773

Sponsors

Hospital Regional de Mato Grosso do Sul
Lead Sponsor
Universidade Federal de Mato Grosso do Sul
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Men and women at least 18 years older with confirmed disease with positive SARS-CoV-2 molecular test (RT-PCR) admitted at Hospital Regional de Mato Grosso do Sul ward with at least one of the following conditions: oxygen saturation less than 95% in ambient air; signs of respiratory discomfort or rise in respiratory frequency evaluated according to age; worsening of underlying disease clinical conditions; hypotension; fespiratory insufficiency.

Exclusion criteria

Exclusion criteria: Viral infections wiht etiological agents other than SARS-CoV-2; negative SARS-CoV-2 molecular test (RT-PCR); other diseases with respiratory tract impairment with negative SARS-CoV-2 molecular test (RT-PCR); need of special treatment and care, such as pregnant women and severe comorbidities (cardiovascular disease, cancer, imunosuppression, HIV and tuberculosis, among others).

Design outcomes

Primary

MeasureTime frame
We expect that the group receiving active homeopathic medicine as complementary therapy will have a more favorable resolution of Covid-19, which will be verified by smaller number of days until the patient is discharged, and for a smaller number of participants belonging to the active group that die or have clinical aggravation requiring transference to the Hospital's Intensive Care Unit.

Secondary

MeasureTime frame
Secondary outcomes are not expected.

Countries

Brazil

Contacts

Public ContactIago Caires
iago.caires.1804@gmail.com+55 16 98185-6481

Outcome results

None listed

Source: REBEC (via WHO ICTRP)