Last reviewed · How we verify

NCT06086093

Evaluate the Efficacy of RespireAidTM in Patient With Externally Contracted Seasonal Epidemic (外感時疫)

Completed NA Last updated 22 December 2023
What this trial tests

NA trial testing RespireAid TM/placebo in Respiration Disorders in 260 participants. Completed in 15 December 2023.

Timeline
7 August 2023
Primary endpoint
11 October 2023
15 December 2023

Quick facts

Lead sponsorSun Ten Pharmaceutical Co., Ltd.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment260
Start date7 August 2023
Primary completion11 October 2023
Estimated completion15 December 2023
Sites2 locations across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Sun Ten Pharmaceutical Co., Ltd.

Who can join

Adults 18 to 79, any sex, with Respiration Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to learn about in the main objective of this study is to evaluate the clinical efficacy of the RespireAidTM (Tai-wan-Qing-Guan-Yi-Hao) to ease the symptoms of fever, sore throat, and cough, and the safety after treatment. Participants will Take 1 sachet(5g) 4 times daily. There is a comparison group: Researchers will compare placebo to see if RespireAidTM.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Respiration Disorders

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06086093.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing