Study for clinical oral characteristics of patients with novel coronavirus pneumonia (COVID-19) and Effect of 3% hydrogen peroxide gargle on the Intraoral novel coronavirus

Study for the effect of 3% hydrogen peroxide gargle on the Intraoral novel coronavirus of the patients with novel coronavirus pneumonia (COVID-19)

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000030539

Enrollment

Unknown

Registered

2020-03-06

Start date

2020-03-06

Completion date

Unknown

Last updated

2020-03-23

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

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

control group:None

Experimental group (mild and normal type in patients with new coronavirus pneumonia):3% hydrogen peroxide gargle

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Pharyngeal swabs are used to detect the positive nucleic acid of the novel coronavirus, or the virus gene sequencing is highly homologous with the known novel coronavirus; 2. Ages between 18 to 85 years male or female; 3. Subjects should fully understand the purpose, nature, methods and reactions of the experiment, voluntarily participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with mental illness who cannot cooperate with the sampling; 2. Patients judged by the researchers as unsuitable for the study.

Design outcomes

Primary

Measure	Time frame
novel coronavirus nucleic acid;	—

Countries

China

Contacts

Public ContactFan Zhong

Guangzhou Eighth People's Hospital

gz8hzf@126.com+86 18122317900

Outcome results

None listed

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