Effect of Gui-Lu-Er-Xian-Jiao-Wan on Intradialytic Hypotension
Primary Purpose
Intradialytic Hypotension
Status
Not yet recruiting
Phase
Phase 2
Locations
Taiwan
Study Type
Interventional
Intervention
Gui-Lu-Er-Xian-Jiao-Wan
Sponsored by
About this trial
This is an interventional treatment trial for Intradialytic Hypotension focused on measuring Intradialytic Hypotension, Chinese herbal medicine, Gui-Lu-Er-Xian-Jiao
Eligibility Criteria
Inclusion Criteria:
- End stage renal disease treated with hemodialysis for ≥3 months
- Receive a standard thrice-weekly hemodialysis schedule
- More than 25% of hemodialysis sessions complicated by intradialytic hypotension
Exclusion Criteria:
- Active malignancy
- Life-threatening conditions
- Pregnancy
- Recent participation in another clinical trial for intradialytic hypotension
- History of hypersensitivity or contraindication to herbal medicine
Sites / Locations
- Kaohsiung Chang Gung Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Group A
Group B
Arm Description
Gui-Lu-Er-Xian-Jiao-Wan (GLEXJW) 3g orally twice daily for 12 weeks.
No intervention.
Outcomes
Primary Outcome Measures
Intradialytic hypotension episode
Hypotension episode during hemodialysis
Secondary Outcome Measures
Early termination of hemodialysis
The episode of early termination in hemodialysis due to hypotension
SF-36
Short Form (36) Health Survey (SF-36)
Full Information
NCT ID
NCT05517993
First Posted
August 24, 2022
Last Updated
August 24, 2022
Sponsor
Chang Gung Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05517993
Brief Title
Effect of Gui-Lu-Er-Xian-Jiao-Wan on Intradialytic Hypotension
Official Title
Effect of Gui-Lu-Er-Xian-Jiao-Wan on Intradialytic Hypotension: a Randomized Crossover Pilot Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2022 (Anticipated)
Primary Completion Date
July 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Intradialytic hypotension (IDH), a common complication during hemodialysis (HD) could increase patients' morbidity and mortality. Previous studies considered that some Chinese herbal medicine (CHM) plays a complementary role in reducing the frequency of IDH. This trial is aimed to investigate the effect of Gui-Lu-Er-Xian-Jiao-Wan (GLEXJW) in patients with intradialytic hypotension.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intradialytic Hypotension
Keywords
Intradialytic Hypotension, Chinese herbal medicine, Gui-Lu-Er-Xian-Jiao
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group A
Arm Type
Experimental
Arm Description
Gui-Lu-Er-Xian-Jiao-Wan (GLEXJW) 3g orally twice daily for 12 weeks.
Arm Title
Group B
Arm Type
No Intervention
Arm Description
No intervention.
Intervention Type
Drug
Intervention Name(s)
Gui-Lu-Er-Xian-Jiao-Wan
Other Intervention Name(s)
GLEXJW
Intervention Description
Gui-Lu-Er-Xian-Jiao-Wan (GLEXJW) is an ancient CHM formula, mainly originating from processed tortoise shells, antlers, Ginseng, and wolfberry.
Primary Outcome Measure Information:
Title
Intradialytic hypotension episode
Description
Hypotension episode during hemodialysis
Time Frame
Each time of dialysis during 12-weeks study period.
Secondary Outcome Measure Information:
Title
Early termination of hemodialysis
Description
The episode of early termination in hemodialysis due to hypotension
Time Frame
Each time of dialysis during 12-weeks study period.
Title
SF-36
Description
Short Form (36) Health Survey (SF-36)
Time Frame
Baseline, 12 weeks, 28 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
End stage renal disease treated with hemodialysis for ≥3 months
Receive a standard thrice-weekly hemodialysis schedule
More than 25% of hemodialysis sessions complicated by intradialytic hypotension
Exclusion Criteria:
Active malignancy
Life-threatening conditions
Pregnancy
Recent participation in another clinical trial for intradialytic hypotension
History of hypersensitivity or contraindication to herbal medicine
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chun-Ting Liu
Phone
+88677317123
Email
juntin0214@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chun-Ting Liu
Organizational Affiliation
Chang Gung Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kaohsiung Chang Gung Memorial Hospital
City
Kaohsiung
ZIP/Postal Code
833
Country
Taiwan
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effect of Gui-Lu-Er-Xian-Jiao-Wan on Intradialytic Hypotension
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