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Acupuncture for Chemical Therapy Induced Nausea and Vomiting

Primary Purpose

Chemotherapy-induced Nausea and Vomiting

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Manual acupuncture implemented by senior acupuncturists
Manual acupuncture implemented by junior acupuncturists
Manual acupuncture on P6 point
Sponsored by
Beijing University of Chinese Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chemotherapy-induced Nausea and Vomiting focused on measuring Acupuncture, Expertise-based randomized controlled trial, Nausea, Vomiting, Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Confirmed diagnosis of cancer
  • Must receive cancer chemotherapy containing cisplatin
  • Use 5-TH receptor antagonists as an antiemetic drug in the chemotherapy duration

Exclusion Criteria:

  • Concurrent neoplasms or illness that induces nausea independent of chemotherapy
  • Received acupuncture treatments for other conditions less than 4 weeks before chemotherapy treatment
  • Severe infection
  • Severe heart, liver, kidney and brain diseases
  • Cardiac pacemaker
  • Radiotherapy or hormone therapy during chemotherapy treatments

Sites / Locations

  • Dongzhimen Hospital, Beijing University of Chinese medicine
  • Guanganmen Hospital,China Academy of Chinese Medical Sciences
  • Xiyuan Hospital, China Academy of Chinese Medical Sciences

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

No Intervention

Arm Label

A(senior acupuncturists)

B(junior acupuncturists)

C(P6 points)

D(no acupuncture)

Arm Description

Manual acupuncture implemented by senior acupuncturists (clinical experience >15 years)

Manual acupuncture implemented by junior acupuncturists (clinical experience <5 years)

Manual acupuncture on P6 points by junior acupuncturists (clinical experience <5 years)

No acupuncture treatment

Outcomes

Primary Outcome Measures

NCI nausea and vomiting rating scale
Rhodes Scale

Secondary Outcome Measures

Global assessment on effectiveness by patients (a single direct question with five levels of alternatives)
Patients' confidence towards acupuncture treatment (a single direct question with five levels of alternatives)
Consumption of additional antiemetic

Full Information

First Posted
July 16, 2016
Last Updated
July 20, 2016
Sponsor
Beijing University of Chinese Medicine
Collaborators
Dongzhimen Hospital, Beijing, Guang'anmen Hospital of China Academy of Chinese Medical Sciences, Xiyuan Hospital of China Academy of Chinese Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02842307
Brief Title
Acupuncture for Chemical Therapy Induced Nausea and Vomiting
Official Title
Impact of Acupuncturist Expertise on Clinical Effectiveness for Chemotherapy Induced Nausea and Vomiting in Cancer Patients: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing University of Chinese Medicine
Collaborators
Dongzhimen Hospital, Beijing, Guang'anmen Hospital of China Academy of Chinese Medical Sciences, Xiyuan Hospital of China Academy of Chinese Medical Sciences

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is an expertise-based randomized controlled trial. The hypothesis of this study is that the differences in expertise of acupuncturist may impact clinical effect. In this study, patients will be randomized to 4 group, receiving the treatment from senior acupuncturist, junior acupuncturist, junior acupuncturist by only acupuncture Neiguan(P6), or not receive the acupuncture. All patients receive the basic cisplatin chemotherapy. The duration of treatment is from the first day receiving cisplatin until two days after cisplatin on each group. NCI and Rhode scale will be used to measure the control of nausea and vomiting.
Detailed Description
This is an expertise-based randomized controlled trial. The hypothesis of this study is that the differences in expertise of acupuncturist may impact clinical effect. In this study, 102 patients will be randomly divided into 4 groups which separately receiving the treatment from senior acupuncturist(clinical experience> 15 years, considered in this trial as highly expertised), junior acupuncturist(clinical experience< 5 years, considered in this trial as lower expertised), junior acupuncturist only acupuncture Neiguan(P6), or not receiving the acupuncture. All participants receive the cisplatin-based chemotherapy and 5-HT3 as antiemetic treatment will be included. Acupuncture treatments are given once daily, the duration of treatment is from the first day receiving cisplatin until two days after cisplatin. NCI and Rhode scale will be used to measure the control of nausea and vomiting. only outcome assessors are blinded. Generalized estimating equations will be used to compare the effects among groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chemotherapy-induced Nausea and Vomiting
Keywords
Acupuncture, Expertise-based randomized controlled trial, Nausea, Vomiting, Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
102 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A(senior acupuncturists)
Arm Type
Active Comparator
Arm Description
Manual acupuncture implemented by senior acupuncturists (clinical experience >15 years)
Arm Title
B(junior acupuncturists)
Arm Type
Active Comparator
Arm Description
Manual acupuncture implemented by junior acupuncturists (clinical experience <5 years)
Arm Title
C(P6 points)
Arm Type
Active Comparator
Arm Description
Manual acupuncture on P6 points by junior acupuncturists (clinical experience <5 years)
Arm Title
D(no acupuncture)
Arm Type
No Intervention
Arm Description
No acupuncture treatment
Intervention Type
Procedure
Intervention Name(s)
Manual acupuncture implemented by senior acupuncturists
Other Intervention Name(s)
Traditional manual acupuncture, Traditional acupuncture
Intervention Description
Manual acupuncture once per day. No limitation on points, manipulations and time per session. Senior acupuncturists have to have more than 15 years of acupuncture clinical practice experience.
Intervention Type
Procedure
Intervention Name(s)
Manual acupuncture implemented by junior acupuncturists
Other Intervention Name(s)
Traditional manual acupuncture, Traditional acupuncture
Intervention Description
Manual acupuncture once per day. No limitation on points, manipulations and time per session. Junior acupuncturists have to have less than 5 years of acupuncture clinical practice experience.
Intervention Type
Procedure
Intervention Name(s)
Manual acupuncture on P6 point
Other Intervention Name(s)
Traditional manual acupuncture, Traditional acupuncture
Intervention Description
Manual acupuncture implemented by junior acupuncturists once per day. P6 point, bilaterally, should achieve deqi sensation by even manipulations. Junior acupuncturists have to have less than 5 years of acupuncture clinical practice experience.
Primary Outcome Measure Information:
Title
NCI nausea and vomiting rating scale
Time Frame
From the first day receiving cisplatin until two days after cisplatin in each group
Title
Rhodes Scale
Time Frame
From the first day receiving cisplatin until two days after cisplatin in each group
Secondary Outcome Measure Information:
Title
Global assessment on effectiveness by patients (a single direct question with five levels of alternatives)
Time Frame
The second day after cisplatin
Title
Patients' confidence towards acupuncture treatment (a single direct question with five levels of alternatives)
Time Frame
The first day receiving cisplatin and the second day after cisplatin
Title
Consumption of additional antiemetic
Time Frame
From the first day receiving cisplatin until two days after cisplatin
Other Pre-specified Outcome Measures:
Title
Acupuncture related adverse events
Time Frame
From the first day receiving cisplatin until two days after cisplatin
Title
Adverse events
Time Frame
From the first day receiving cisplatin until two days after cisplatin

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed diagnosis of cancer Must receive cancer chemotherapy containing cisplatin Use 5-TH receptor antagonists as an antiemetic drug in the chemotherapy duration Exclusion Criteria: Concurrent neoplasms or illness that induces nausea independent of chemotherapy Received acupuncture treatments for other conditions less than 4 weeks before chemotherapy treatment Severe infection Severe heart, liver, kidney and brain diseases Cardiac pacemaker Radiotherapy or hormone therapy during chemotherapy treatments
Facility Information:
Facility Name
Dongzhimen Hospital, Beijing University of Chinese medicine
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100007
Country
China
Facility Name
Guanganmen Hospital,China Academy of Chinese Medical Sciences
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100053
Country
China
Facility Name
Xiyuan Hospital, China Academy of Chinese Medical Sciences
City
Beijing
ZIP/Postal Code
100091
Country
China

12. IPD Sharing Statement

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Acupuncture for Chemical Therapy Induced Nausea and Vomiting

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