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Efficacy of Kangliuwan for Recurrent Grade IV Glioma

Efficacy of Hospital Traditional Chinese Medicine Preparation Kangliuwan for Recurrent Grade IV Glioma: A Prospective Exploratory Clinical Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03949192
Enrollment
20
Registered
2019-05-14
Start date
2019-06-28
Completion date
2021-06-30
Last updated
2020-05-05

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

Conditions

Glioma of Brain, Recurrence

Brief summary

A Prospective Exploratory Clinical Study to explore the efficacy of Hospital Traditional Chinese Medicine Preparation Kangliuwan for Recurrent Grade IV Glioma.

Interventions

None listed

Sponsors

Xuanwu Hospital, Beijing
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. The patient signed informed consent voluntarily; 2. The age of patient is between 18 and 80 years; 3. KPS score ≥40 ; The patient has normal liver and kidney function Normal heart function Better follow-up and compliance;

Exclusion criteria

1. The patient did not sign informed consent or signed unvoluntarily. 2. Non-glioma patients 3. Active infection 4. Human immunodeficiency virus (HIV) positive 5. Hepatitis C or hepatitis B infective 6. Pregnancy or breast-feeding women 7. Patients did not agree to use effective contraception during treatment and the following 3 months. 8. Patients also participated in other clinical studies. 9. The subjects researchers believe are not suitable for participation or completion of the study.

Design outcomes

Primary

MeasureTime frameDescription
Changes in tumor volume3 monthsthe volume of tumor decreased after taking Kangliuwan

Countries

China

Contacts

Primary ContactQingtang Lin, MD. Ph.D
linqingtang@xwhosp.orn8610-83198362
Backup ContactGe Sun, B.A.
sunge0923@126.com8610-83198362

Outcome results

None listed

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