search
Back to results

To Evaluate the Effects of Heating Device (Electronic Moxibustion) in Patients With Intradialytic Hypotension

Primary Purpose

Hemodialysis-Induced Symptom, Intra-dialytic Hypotension

Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
"HEALTHY BOX" Powered heating pad (electronic moxibustion)
Sponsored by
Chang Gung Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Hemodialysis-Induced Symptom focused on measuring hemodialysis, Intra-dialytic Hypotension, heating device, electronic moxibustion

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age between 20 to 80-years-old
  2. Willing to sign inform consent
  3. Weekly hemodialysis 3 times per week, each time at least 180 minutes
  4. During the past 2 months of hemodialysis, there is symptomatic intra-dialytic hypotension for over 15% of the time or under regular use of Midodrine.

Exclusion Criteria:

  1. Pregnancy or breast-feeding
  2. Not able to fill out questionnaires
  3. Severe comorbidities, including cirrhosis, heart failure, autoimmune diseases and cancer
  4. Diabetic peripheral neuropathy or patients insensitive to heat or unable to effectively express themselves in heated situations
  5. Undergoing other types of alternative treatment, including Chinese medicine and regional remedies.

Sites / Locations

  • Keelung Chang Gung Memorial Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Group 1

Group 2

Arm Description

For Group 1, each subject will receive Treatment 1# first. Then, it takes 2-week washout period with regular dialysis 3 times per week and then receive Treatment 2#. Treatment 1# will be regular dialysis 3 times per week for 4 weeks. Treatment 2# will be regular dialysis 3 times per week plus "HEALTHY BOX" Powered heating pad on acupoint CV4 at the abdomen for 1 hour during dialysis, also for 4 weeks.

For Group 2, each subject will receive Treatment 2# first. Then, it takes 2-week washout period with regular dialysis 3 times per week and then receive Treatment 1#. Treatment 2# will be regular dialysis 3 times per week plus "HEALTHY BOX" Powered heating pad on acupoint CV4 at the abdomen for 1 hour during dialysis, also for 4 weeks. Treatment 1# will be regular dialysis 3 times per week for 4 weeks.

Outcomes

Primary Outcome Measures

change of frequency of IDH episodes
times of IDH episode according to NADIR, KDOQI criteria
change of number of nursing interventions during HD
Trendelenburg position, man¬ual reduction of ultrafiltration rate, infusion of isotonic saline or hypertonic fluid, lowering of dialysate temperature

Secondary Outcome Measures

change of the degree of cold intolerance
from 0 to 100; 0 is not cold, 100 is very cold
change of the degree of fatigue after dialysis
scores from 0-10;0 is not tired, 10 is very tired
blood pressure changes
systolic, diastolic blood pressure and mean arterial pressure: mmHg
change of recovery time from fatigue after dialysis
within minutes (0), when arriving home (0), at bedtime (2), the next morning (5), and by next HD (10)

Full Information

First Posted
February 11, 2019
Last Updated
September 10, 2021
Sponsor
Chang Gung Memorial Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT03856151
Brief Title
To Evaluate the Effects of Heating Device (Electronic Moxibustion) in Patients With Intradialytic Hypotension
Official Title
To Evaluate the Effects of Heating Device (Electronic Moxibustion) in Patients With Intradialytic Hypotension
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
April 17, 2019 (Actual)
Primary Completion Date
April 20, 2020 (Actual)
Study Completion Date
April 28, 2021 (Actual)

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
The aim of this study is to investigate the effects of heating device among otherwise stable patients with intradialytic hypotension
Detailed Description
Intradialytic hypotension (IDH) is a common complication during hemodialysis (HD) which accounts up to 5 to 30 percent of all dialysis treatment and is associated with increased morbidity and mortality. The etiology of IDH is multifactorial, but intravascular volume depletion, autonomic neuropathy, and decreased cardiac reserve were the main factors. Several approaches were utilized to prevent IDH including adaptation of dialysis prescriptions, lengthening in dialysis time, avoiding food intake during dialysis, as well as limiting interdialytic sodium intake and administration of vasoconstrictor agents. However, it remains necessary to seek novel effective and safe inventions for IDH. To date, no studies have been done to evaluate the effectiveness of acupuncture and traditional moxibustion during HD for safety reasons (eg: risk of bleeding, burns and unpleasant smell). Therefore, the heating device appears to be a non-invasive and safe method for treating IDH. The investigators conduct a clinical trial using infrared heating devices without direct contact to the skin on low temperatures (56±8℃) in treating patients with IDH. 30 eligible participants diagnosed with IDH will be enrolled and divided into Group 1 and Group 2. Treatment 1# will be regular dialysis 3 times per week for 4 weeks. Treatment 2# will be regular dialysis 3 times per week plus "HEALTHY BOX" Powered heating pad on acupoint CV4 at the abdomen for 1 hour during dialysis, also for 4 weeks. For Group 1, each subject will receive Treatment 1# first, for Group 2, Treatment 2# will be received first. Then, it takes 2-week washout period with regular dialysis 3 times per week and make Group 1 and Group 2 crossover. Outcomes will include blood pressure changes, nursing intervention frequencies, IDH frequencies, the degree of cold intolerance, the degree of fatigue after dialysis and recovery time from fatigue after dialysis, the percentage of target ultrafiltration achieved and blood biochemistry. Data will be collected at the beginning of the study (baseline), end of Treatment 1 # , and end of Treatment 2#. Subjective questionnaires will be collected before and after each treatment period. The difference of evaluation scores between baseline and post-treatment will be analyzed using generalized linear mixed model. A value of P < 0.05 will be regarded as statistically significant for the above statistical analyses.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemodialysis-Induced Symptom, Intra-dialytic Hypotension
Keywords
hemodialysis, Intra-dialytic Hypotension, heating device, electronic moxibustion

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
30 eligible participants diagnosed with IDH will be enrolled and divided randomly and equally into Group 1 and Group 2 . Treatment 1# will be regular dialysis 3 times per week for 4 weeks. Treatment 2# will be regular dialysis 3 times per week plus "HEALTHY BOX" Powered heating pad on acupoint CV4 at the abdomen for 1 hour during dialysis, also for 4 weeks. For Group 1, each subject will receive Treatment 1# first, for Group 2, Treatment 2# will be received first. Then, a 2-week washout period with regular dialysis 3 times per week will be carried out. Group 1 will then receive Treatment 2# and Group 2 will then receive Treatment 1#. Subjective questionnaires will be done before and after each Treatment period.
Masking
Participant
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Active Comparator
Arm Description
For Group 1, each subject will receive Treatment 1# first. Then, it takes 2-week washout period with regular dialysis 3 times per week and then receive Treatment 2#. Treatment 1# will be regular dialysis 3 times per week for 4 weeks. Treatment 2# will be regular dialysis 3 times per week plus "HEALTHY BOX" Powered heating pad on acupoint CV4 at the abdomen for 1 hour during dialysis, also for 4 weeks.
Arm Title
Group 2
Arm Type
Active Comparator
Arm Description
For Group 2, each subject will receive Treatment 2# first. Then, it takes 2-week washout period with regular dialysis 3 times per week and then receive Treatment 1#. Treatment 2# will be regular dialysis 3 times per week plus "HEALTHY BOX" Powered heating pad on acupoint CV4 at the abdomen for 1 hour during dialysis, also for 4 weeks. Treatment 1# will be regular dialysis 3 times per week for 4 weeks.
Intervention Type
Device
Intervention Name(s)
"HEALTHY BOX" Powered heating pad (electronic moxibustion)
Intervention Description
Using heating pad (electronic moxibustion) with insulating materials on low temperatures (56±8℃) in treating patients with intra-dialytic hypotension
Primary Outcome Measure Information:
Title
change of frequency of IDH episodes
Description
times of IDH episode according to NADIR, KDOQI criteria
Time Frame
baseline, Treatment 1, Treatment 2
Title
change of number of nursing interventions during HD
Description
Trendelenburg position, man¬ual reduction of ultrafiltration rate, infusion of isotonic saline or hypertonic fluid, lowering of dialysate temperature
Time Frame
baseline, Treatment 1, Treatment 2
Secondary Outcome Measure Information:
Title
change of the degree of cold intolerance
Description
from 0 to 100; 0 is not cold, 100 is very cold
Time Frame
week 0,4,6,10
Title
change of the degree of fatigue after dialysis
Description
scores from 0-10;0 is not tired, 10 is very tired
Time Frame
before and after Treatment1 & 2
Title
blood pressure changes
Description
systolic, diastolic blood pressure and mean arterial pressure: mmHg
Time Frame
baseline, Treatment 1, Treatment 2
Title
change of recovery time from fatigue after dialysis
Description
within minutes (0), when arriving home (0), at bedtime (2), the next morning (5), and by next HD (10)
Time Frame
before and after Treatment1 & 2

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: Age between 20 to 80-years-old Willing to sign inform consent Weekly hemodialysis 3 times per week, each time at least 180 minutes During the past 2 months of hemodialysis, there is symptomatic intra-dialytic hypotension for over 15% of the time or under regular use of Midodrine. Exclusion Criteria: Pregnancy or breast-feeding Not able to fill out questionnaires Severe comorbidities, including cirrhosis, heart failure, autoimmune diseases and cancer Diabetic peripheral neuropathy or patients insensitive to heat or unable to effectively express themselves in heated situations Undergoing other types of alternative treatment, including Chinese medicine and regional remedies.
Facility Information:
Facility Name
Keelung Chang Gung Memorial Hospital
City
Keelung
ZIP/Postal Code
20401
Country
Taiwan

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There will be a research number representing the identity. This number will not display the name, ID number, and address. For the results and diagnosis of the visit, the research host will maintain a confidential attitude and carefully maintain the privacy. If research results are published, the identity will remain confidential. Please also understand that if the participant signs the consent form, the participant agrees that the visit record can be directly reviewed by the monitor, auditor, research ethics committee and the competent authority to ensure that the research process and data comply with relevant laws and regulations. These people also promise not to violate the confidentiality of your identity.

Learn more about this trial

To Evaluate the Effects of Heating Device (Electronic Moxibustion) in Patients With Intradialytic Hypotension

We'll reach out to this number within 24 hrs