NVCI: Auriculotherapy and Acupuncture's Treatment for Chemotherapy-induced Nausea and Vomiting (CINV)

Sponsor
Hopital Foch (Other)
Overall Status
Completed
CT.gov ID
NCT02767791
Collaborator
(none)
116
5
4
61.1
23.2
0.4

Study Details

Study Description

Brief Summary

The management of chemotherapy-induced nausea and vomiting (CINV) has evolved in recent years and became less frequent. CINV include early (occurring within 24 hours of chemotherapy administration) and delayed (occurring within 4 days after chemotherapy) nausea and vomiting.

Preventive treatment, such as Glucocorticoids, 5-hydroxytryptamine type 3 (5-HT3) receptor antagonists and neurokinin 1 (NK1) receptor antagonists, are administered according to the classification in 4 grades of expected CINV

  • Very low: <10% occurrence of CINV;

  • Low: 10 to 30% occurrence of CINV;

  • Average: 30 to 90% occurrence of CINV;

  • High: > 90% occurrence of CINV. These treatments have been the subject of recommendations. Despite these available treatments, some patients still complain of vomiting, or more frequently nausea and loss of appetite.

Meanwhile, Chinese acupuncture has proven effective on the prevention of CINV as complementary treatment, mainly in the acute phase and to a lesser extent in the delayed phase. The most common points are Pericardium 6 (wrist) treated with conventional acupuncture needles, electro-acupuncture or acupressure.

Auriculotherapy (ear acupuncture) has proven effective on nausea of pregnancy and postoperative nausea, but, to our knowledge, there are no studies published on the effect of auriculotherapy on CINV.

These complementary treatments have virtually no side effects. In our institution, a simple treatment of acupuncture (2 points Pericardium 6 treated) and auriculotherapy (2 auricular point treated) is regularly use in patients who present CINV despite preventive treatment and most of them are relieved.

The investigators propose a clinical trial in this population to assess symptoms improvement in patients presenting CINV after their first administration of chemotherapy despite adapted preventive treatment. Experimental treatment with semi-permanent needles takes place during administration of the second session of chemotherapy. CINV are evaluated through the (MAT) score that measures the frequency and intensity of nausea and vomiting in the 24 hours following the session and during the 4 days after administration Chemotherapy.

Multinational Association of Supportive Care in Cancer Antiemesis Tool (MASCC), Http://www.MASCC.org/.

Condition or Disease Intervention/Treatment Phase
  • Other: Acupuncture
  • Other: Auriculotherapy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
116 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Auriculotherapy and Acupuncture's Treatment for Chemotherapy-induced Nausea and Vomiting (CINV)
Actual Study Start Date :
May 4, 2016
Actual Primary Completion Date :
Jun 7, 2021
Actual Study Completion Date :
Jun 7, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Acupuncture

Acupuncture wrist 6

Other: Acupuncture
Acupuncture

Active Comparator: Auriculotherapy

Auriculotherapy

Other: Auriculotherapy
Auriculotherapy

Experimental: Auriculotherapy and acupuncture

Auriculotherapy and acupuncture

Other: Acupuncture
Acupuncture

Other: Auriculotherapy
Auriculotherapy

No Intervention: No treatment

No treatment

Outcome Measures

Primary Outcome Measures

  1. Digital Scale for nausea [1 day]

    Digital Scale for nausea (H24 MAT score)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • out-patient chemotherapy

  • treated nausea vomiting induced by chemotherapy (NVIC)

Exclusion Criteria:
  • prior treatment with acupuncture and or auriculotherapy for NVIC

  • no conventional treatment for NVIC like phytotherapy and homeopathy

  • radiotherapy (five days before and 5 days after chemotherapy)

  • MRI in the five days after first visit

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre hospitalier de Gonesse Gonesse France
2 René Huguenin Saint-Cloud France
3 Centre spécilaisé en cancérologie Paris Nord Sarcelles France 95200
4 Clinique de l'Estrée Stains France
5 Hopital Foch Suresnes France 92150

Sponsors and Collaborators

  • Hopital Foch

Investigators

  • Principal Investigator: Mireille Michel-Cherqui, MD, Hopital Foch

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hopital Foch
ClinicalTrials.gov Identifier:
NCT02767791
Other Study ID Numbers:
  • 2015/34
  • 2015-A01988-41
First Posted:
May 10, 2016
Last Update Posted:
Sep 1, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 1, 2021