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CompletedNCT01503346TCMUpdated Feb 17, 2020

DaHuang GangTsao Tang to Improve the Appetite Loss Condition of Cancer Patients

A Phase 2 interventional study of DaHuang GanTsao Tang in Non-organic Loss of Appetite, sponsored by Changhua Christian Hospital. Completed at 1 site in Taiwan. Open to participants aged 20 Years to 80 Years. Per ClinicalTrials.gov, last updated 2020-02-17.

Sponsored by Changhua Christian Hospital · Phase 2, Interventional, and Supportive care

Phase
Phase 2
Study type
Interventional
Enrollment
4
Allocation
Not applicable
Ages
20 Years to 80 Years
Sex
All
01

Study summary

Appetite loss is a severe and common symptom among late-stage cancer patients, and it causes great the anxiety for the patient's family. In TCM theory, the investigators call these patients are in block and repulsion condition. The investigators try to set a study to use the herbal medicine solution taken in frequent small amounts by cancer patients in late-stage to improve the appetite loss condition. Through this method, the investigators not only want to improve the quality of life of cancer patients in late-stage but also set a valuable treatment.

Read the detailed description

Intervention group

    1. 2 grams of DaHuang abstract powder and 0.5 grams GanTsao abstract powder are mixed and separated into four packages;
    1. each package was given to each patient four times a day (three time after meal and one time before sleep);
    1. each patient received the usual medication of the hospice ward at the same time;
    1. record the patients' score of pre-test, mid-test and after-test of QIPCTP at the 1st day, the 3rd day and the 6th day;
    1. record the patients' score of EORTC QLQ-C30 V3.0 and ECOG (Eastern Cooperative Oncology Group Performance Status) at the 1st day and the 6th day.

Control group

    1. each patient received the usual medication of the hospice ward during the trial interval;
    1. record the patients' score of receive pre-test, mid-test and after-test of QIPCTP at the 1st day, the 3rd day and the 6th day;
    1. record the patients' score of EORTC QLQ-C30 V3.0 and ECOG (Eastern Cooperative Oncology Group Performance Status) at at the 1st day and the 6th day.

Medicine DaHuang herbal abstract powder is produced by Sun Ten Pharmaceutical Co., Ltd, and it's product serial number: 276001. GanCao herbal abstract powder is also produced by Sun Ten Pharmaceutical Co., Ltd, and it's product serial number: 185645. Each herbal abstract powder is qualified with the data of HPLC to confirm each content and stability. The pharmaceutical company is qualified by Good Manufacturing Practice (GMP) certification in Taiwan.

02

Conditions studied

  • Non-organic Loss of Appetite

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Keywords

  • Appetite Loss
03

In context

Anorexia

411 studies on the registry are indexed under Anorexia; 67 are open to participants now.

This study's enrollment of 4 is below the median of 41 across 287 interventional studies indexed under Anorexia.

Browse Anorexia studies →

Lead sponsor

Changhua Christian Hospital is the lead sponsor of 74 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Terminal cancer patients in hospice ward
  • Patients with appetite loss condition
  • Ages between 20 to 80 years old
  • No history of diabetes

Exclusion criteria

Exclusion Criteria:

  • Entered the stage of dying patients
  • Receiving other traditional Chinese medicine
05

Study design

Phase
Phase 2
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
4 participants (actual)

Study arms

  • Experimental
    herbal medicine

    Intervention group * 1. 2 grams of DaHuang abstract powder and 0.5 grams GanTsao abstract powder are mixed and separated into four packages; * 2. each package was given to each patient four times a day (three time after meal and one time before sleep); * 3. each patient received the usual medication of the hospice ward at the same time; * 4. record the patients' score of pre-test, mid-test and after-test of QIPCTP at the 1st day, the 3rd day and the 6th day; * 5. record the patients' score of EORTC QLQ-C30 V3.0 and ECOG (Eastern Cooperative Oncology Group Performance Status) at the 1st day and the 6th day.

    Drug: DaHuang GanTsao Tang

Interventions

  • DrugDaHuang GanTsao Tang

    Intervention group 1. 2 grams of DaHuang abstract powder and 0.5 grams GanTsao abstract powder are mixed and separated into four packages; 2. each package was given to each patient four times a day (three time after meal and one time before sleep); 3. each patient received the usual medication of the hospice ward at the same time; 4. record the patients' score of pre-test, mid-test and after-test of QIPCTP at the 1st day, the 3rd day and the 6th day; 5. record the patients' score of EORTC QLQ-C30 V3.0 and ECOG (Eastern Cooperative Oncology Group Performance Status) at the 1st day and the 6th day.

    Also known as: Herbal Medicine Group

06

What researchers measure

Primary outcomes

  1. appetite score

    The investigators detect the patients' appetite condition at the 1st,3rd and 6th day.

    Time frame: 6 days

07

Study locations

1 site
  • Changhua Christan Hospital
    Changhua City, Changhua Country 500, Taiwan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 17, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01503346
Lead sponsor
Changhua Christian Hospital
Responsible party
Sponsor
First posted
Jan 4, 2012
Start date
Mar 2011
Primary completion
Sep 2011
Completion
Mar 2013
Last update
Feb 17, 2020

Study contacts

Yu De LIU, Master
study chair · Changhua Christian Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.

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