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NCT04031651

Key Specialized Monitoring of Clinical Safety of Pudilan Xiaoyan Oral Liquid in the Real World

Status unknown Last updated 24 July 2019
What this trial tests

trial testing Pudilan Xiaoyan Oral Liquid in Respiratory Infectious Diseases in 10,000 participants. Status unknown.

Timeline
17 July 2019
Primary endpoint
17 July 2019
31 December 2021

Quick facts

Lead sponsorChina Academy of Chinese Medical Sciences
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment10,000
Start date17 July 2019
Primary completion17 July 2019
Estimated completion31 December 2021

Drugs / interventions tested

Conditions studied

Sponsor

China Academy of Chinese Medical Sciences — full company profile →

Who can join

Adults 18 to 80, any sex, with Respiratory Infectious Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To obtain the characteristics of adverse reactions/incidents, analyze the influencing factors and calculate the incidence of adverse reactions/incidents monitored by Pudilan Xiaoyan Oral Liquid in key specialties in the real world, so as to provide a basis for clinical safe and rational drug use.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Clinical Safety of Pudilan Xiaoyan Oral Liquid for the Treatment of Upper Respiratory Tract Infection in the Real World: Protocol for a Prospective, Observational, Registry Study.
    Wang M, Wang L, Liu F, Chen R, et al · · 2025 · PMID 40117581 · DOI 10.2196/65789

Verify or expand the search:

Other recruiting trials for Respiratory Infectious Diseases

Currently open trials in the same condition.

Other China Academy of Chinese Medical Sciences trials

Trials by the same sponsor.

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