Efficacy of a Pelargonium sidoides preparation in patients with the upper respiratory infection

Efficacy of a Pelargonium sidoides preparation in patients with the upper respiratory infection - Efficacy of a Pelargonium sidoides preparationin patients with the upper respiratory infection

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000003815

Enrollment

200

Registered

2010-07-29

Start date

2010-07-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

upper respiratory infection

Interventions

Pelargonium sidoides extract July.-Aug.2010 30drops tid p.o.(10days) Placebo July.-Aug.2010 30drops tid p.o.(10days)

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1-65 years old who diagnosed acute upper respiratory infection. Person who fills following criteria. 1.Upper respiratory tract infection within two days from the appearance of disease. 2.No streptococcal infection 3.Neither taking antibiotics nor antiviral medicine. 4.No immunodeficient condition.

Exclusion criteria

Exclusion criteria: 1.Patient who is dementia, visual impairment,unable to answer, unable to fill in. 2.Investigation is refused by a patient. 3.Allergy to the medicine. 4.When a doctor recognize not suitable

Design outcomes

Primary

Measure	Time frame
Cold intensity score(CIS)	—

Secondary

Measure	Time frame
General Well-Being Index	—

Countries

Japan

Contacts

Public ContactKuniko Nakayama

Kyoritsu general hospital Department of general medicine

kumalawi@yahoo.co.jp052-654-2211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026