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Clinical Trial on Palliative Cancer Patients With Constipation

Primary Purpose

Constipation

Status
Completed
Phase
Phase 2
Locations
Hong Kong
Study Type
Interventional
Intervention
Chinese herbal medicine
Placebo
Sponsored by
Hong Kong Baptist University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Constipation focused on measuring Chinese herbal medicine formula, MaZiRenWan, Randomized controlled trial, Constipation, Palliative care in cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Severity of constipation > 3 points (an 8-point scale from 0 to 7)
  • Palliative Performance Scale ≥60%
  • Relatively stable liver and renal function within 3 months
  • Patients who can read and speak Chinese

Exclusion Criteria:

  • Inability to communicate
  • Presence of a colostomy, or gastrointestinal obstruction
  • Presence of loose or watery stool (Bristol stool scale 6-7) or bowel movement > 3/day under routine laxative treatment
  • History of Chinese herbal medicine allergies
  • Estimated life expectancy less than 1 month

Sites / Locations

  • Caritas Medical Centre
  • Hong Kong Buddhist Hospital
  • Our Lady of Maryknoll Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Chinese herbal medicine

Placebo

Arm Description

MaZiRenWan 10g plus HuangQi 20g are chosen as the core prescription. Furthermore, six herbal granules can be added according to the syndrome differentiated for individual participant. They are ShuDiHuang 15g and Danggui 10g for deficiency of blood, Maidong 15g and ShengDiHuang 10g for deficiency of Yin, and RouCongRong 15g and Niuxi 10g for deficiency of Yang.

Placebo is made from dextrin (76.03%), tea essence (23.61%), gardenin (0.02%), and caramel (0.34%) to achieve color, smell, taste, and texture comparable to the herbal granules.

Outcomes

Primary Outcome Measures

Global symptom improvement (improved / same / worse)
Participants are asked to rate their impression of change in constipation symptoms in comparison with their baseline, with scores from 0 to 6 represents markedly worse or better at the respective extremes. The response categories are collapsed to simply "improved" for score 4-6, "same" for score 3, or "worse" for score 0-2.

Secondary Outcome Measures

Number of bowel movement (times/day)
Stool form
Stool form is assessed with 7-point Bristol Stool Scale (ranging from "separate hard lumps" to "watery")
Extra laxatives used (times/week)
Constipation visual analogue scale
The severity of constipation is evaluated by an eight point ordinal rating scale (0=none to 7=most severe)
Constipation related symptoms
Sensation of straining, incomplete evacuation, bloating, abdominal pain/cramping, nausea, and passing of gas are recorded using a 7-point ordinal scale (0=not at all and 6=very severe)
Adverse events
Blood creatinine level (umol/L)
Blood urea level (mmol/L)
Serum glutamic pyruvic transaminase(SGPT) Level (U/L)
Serum Glutamic Oxaloacetic Transaminase (SGOT) Level (U/L)

Full Information

First Posted
May 25, 2016
Last Updated
August 6, 2018
Sponsor
Hong Kong Baptist University
Collaborators
Caritas Medical Centre, Hong Kong, Yan Chai Hospital, Our Lady of Maryknoll Hospital, Hong Kong Buddhist Hospital, Hospital Authority, Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT02795390
Brief Title
Clinical Trial on Palliative Cancer Patients With Constipation
Official Title
Chinese and Western Medicine Collaborative Studies on Palliative Cancer Patients With Constipation
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
November 2016 (Actual)
Primary Completion Date
August 2018 (Actual)
Study Completion Date
August 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hong Kong Baptist University
Collaborators
Caritas Medical Centre, Hong Kong, Yan Chai Hospital, Our Lady of Maryknoll Hospital, Hong Kong Buddhist Hospital, Hospital Authority, Hong Kong

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
It is a double-blinded, randomized, placebo-controlled trial for advanced cancer patients with constipation. 60 patients will be randomly assigned to have individualized herbal intervention (treatment group) or placebo (control group) in 1:1 ratio. For the treatment group, MaZiRenWan 10g plus HuangQi 20g are chosen as the core prescription. Furthermore, six herbal granules can be added according to the syndrome differentiated for individual participant. Placebo is made from dextrin (76.03%), tea essence (23.61%), gardenin (0.02%), and caramel (0.34%) to achieve color, smell, taste, and texture comparable to the herbal granules. Patients are instructed to dissolve the granules in 150ml of hot water, twice daily for two weeks. The primary end point is the global symptom improvement. Secondary outcome measures include stool frequency, stool form, use of rescue herbal granules, constipation visual analogue scale (CVAS) (0=none to 7=most severe) and individual assessment of constipation related symptoms. For the safety profiles of herbal intervention, the important adverse events reported and clinical laboratory evaluations of liver and renal function are determined.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Constipation
Keywords
Chinese herbal medicine formula, MaZiRenWan, Randomized controlled trial, Constipation, Palliative care in cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Chinese herbal medicine
Arm Type
Experimental
Arm Description
MaZiRenWan 10g plus HuangQi 20g are chosen as the core prescription. Furthermore, six herbal granules can be added according to the syndrome differentiated for individual participant. They are ShuDiHuang 15g and Danggui 10g for deficiency of blood, Maidong 15g and ShengDiHuang 10g for deficiency of Yin, and RouCongRong 15g and Niuxi 10g for deficiency of Yang.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo is made from dextrin (76.03%), tea essence (23.61%), gardenin (0.02%), and caramel (0.34%) to achieve color, smell, taste, and texture comparable to the herbal granules.
Intervention Type
Drug
Intervention Name(s)
Chinese herbal medicine
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Global symptom improvement (improved / same / worse)
Description
Participants are asked to rate their impression of change in constipation symptoms in comparison with their baseline, with scores from 0 to 6 represents markedly worse or better at the respective extremes. The response categories are collapsed to simply "improved" for score 4-6, "same" for score 3, or "worse" for score 0-2.
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Number of bowel movement (times/day)
Time Frame
2 weeks
Title
Stool form
Description
Stool form is assessed with 7-point Bristol Stool Scale (ranging from "separate hard lumps" to "watery")
Time Frame
2 weeks
Title
Extra laxatives used (times/week)
Time Frame
2 week
Title
Constipation visual analogue scale
Description
The severity of constipation is evaluated by an eight point ordinal rating scale (0=none to 7=most severe)
Time Frame
2 weeks
Title
Constipation related symptoms
Description
Sensation of straining, incomplete evacuation, bloating, abdominal pain/cramping, nausea, and passing of gas are recorded using a 7-point ordinal scale (0=not at all and 6=very severe)
Time Frame
2 weeks
Title
Adverse events
Time Frame
2 weeks
Title
Blood creatinine level (umol/L)
Time Frame
2 weeks
Title
Blood urea level (mmol/L)
Time Frame
2 weeks
Title
Serum glutamic pyruvic transaminase(SGPT) Level (U/L)
Time Frame
2 weeks
Title
Serum Glutamic Oxaloacetic Transaminase (SGOT) Level (U/L)
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Severity of constipation > 3 points (an 8-point scale from 0 to 7) Palliative Performance Scale ≥60% Relatively stable liver and renal function within 3 months Patients who can read and speak Chinese Exclusion Criteria: Inability to communicate Presence of a colostomy, or gastrointestinal obstruction Presence of loose or watery stool (Bristol stool scale 6-7) or bowel movement > 3/day under routine laxative treatment History of Chinese herbal medicine allergies Estimated life expectancy less than 1 month
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhao-xiang Bian, PhD
Organizational Affiliation
Hong Kong Baptist University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Caritas Medical Centre
City
Hong Kong
Country
Hong Kong
Facility Name
Hong Kong Buddhist Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Our Lady of Maryknoll Hospital
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Research results will be published after analysis.
IPD Sharing Time Frame
After publication with no time limit
IPD Sharing Access Criteria
Open for public
Citations:
PubMed Identifier
35236375
Citation
Cheng CW, Mok HF, Yau CWS, Chan JTM, Kang YC, Lam PY, Zhong LLD, Zhao C, Ng BFL, Kwok AOL, Tse DMW, Bian ZX. A pilot randomized placebo-controlled study on modified MaZiRenWan: a formulated Chinese medicine to relieve constipation for palliative cancer patients. Chin Med. 2022 Mar 2;17(1):31. doi: 10.1186/s13020-022-00580-0.
Results Reference
derived

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Clinical Trial on Palliative Cancer Patients With Constipation

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