Skip to content

Efficacy and Safety of Abelmoschus Manihot for Chronic Kidney Disease

Efficacy and Safety of Abelmoschus Manihot for Chronic Kidney Disease:a Multicentre Open Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02231138
Enrollment
1600
Registered
2014-09-04
Start date
2014-09-30
Completion date
2016-12-31
Last updated
2016-06-01

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

Conditions

Chronic Kidney Disease

Keywords

Abelmoschus manihot, Chronic Kidney Disease, proteinuria, efficacy, safety

Brief summary

Huangkui Capsule is a single medicament of traditional Chinese medicine consists of Abelmoschus manihot and has been widely used to treat kidney disease. The purpose of this study is to evaluate the safety and efficacy of Abelmoschus manihot for treating chronic kidney disease in large scale samples with long time take.

Detailed description

The test has not been completed.

Interventions

DRUGAbelmoschus manihot (AM)

Abelmoschus manihot (AM): Huanghui capsule (Jiangsu Suzhong Pharmaceutical Group Co., Ltd.), 0.5 g × 30 capsules/box. A huangkui capsule is a single plant drug extract of Flos Abelmoschus manihot.

Sponsors

Jiangsu Suzhong Pharmaceutical Group Co., Ltd.
CollaboratorINDUSTRY
Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosed as non-ESRD chronic kidney disease (stage I-IV) * Blood pressure of ≤140/90mmHg * Obtaining the signed informed consent from patients

Exclusion criteria

* Be allergic to Huangkui Capsule * Combined with severe primary diseases of heart, brain, liver and hematopoietic system and so on, or other serious diseases which can affect the patient's life * Lactation, pregnancy or plans pregnancy during the study period * Participating in another clinical study in the same period

Design outcomes

Primary

MeasureTime frame
Change in 24-h proteinuria from baseline after treatmentBaseline(week 0), week 12, week 24

Secondary

MeasureTime frame
change in the serum creatinine level from baseline after treatmentBaseline(week 0), week 12, week 24
change in the estimated glomerular filtration rate (eGFR) from baseline after treatmentBaseline(week 0), week 12, week 24

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026