Clinical Trials Directory

Trials / Unknown

UnknownNCT05387187

Evaluate the Effect and Safety of Pu Yang Wan Wu Tang and Western Medicine on Chronic Kidney Disease

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Taipei Medical University Hospital · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The indication of Pu Yang Wan Wu Tang is stroke sequelae, such as half body paralysis, aphasia and muscle weakness. Pu Yang Wan Wu Tang is proved to have the effect of protecting nerve and blood vessel, anti-inflammation, anti-coagulation, dilating peripheral vessel, promot-ing micro circulation, improving hemodynamics, and activating central nerve system. Huangqi could attenuate podocyte injury by regulating the expression and distribu-tion of nephrin and podocin. Huangqi and Danggui are associated with fewer infiltra-tion of macrophages and limitation of renal intrinsic cell activation, which may lead to earlier and persistent reduction of proteinuria. This research will use the compound Chinese medicine, Pu Yang Wan Wu Tang. Those treatments combined Western medicine to assess the efficacy and drug safety on the CKD cases. Series of blood and urine were collected regularly during study to prove the role of Chinese medicine in the treatment of CKD, and to assess their drug safety. The final goal of the plan is to establish the new indication of Pu Yang Wan Wu Tang and enhance the interaction and cooperation between Chinese and Western medicine.

Conditions

Interventions

TypeNameDescription
DRUGPu Yang Wan Wu Tang plus PentoxifyllinePu Yang Wan Wu Tang 5g TID Pentoxifylline 100mg TID
DRUGPentoxifyllinePentoxifylline 100mg TID

Timeline

Start date
2022-05-01
Primary completion
2022-05-31
Completion
2023-06-20
First posted
2022-05-24
Last updated
2023-06-26

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT05387187. Inclusion in this directory is not an endorsement.