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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03751566
Other study ID # MOU-001
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 4, 2016
Est. completion date October 4, 2019

Study information

Verified date November 2018
Source Masaryk Memorial Cancer Institute
Contact Renata Hejnová, Msc
Phone +42054313
Email renata.hejnova@mou.cz
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to evaluate the benefit of the acupuncture as healing modalities in the therapy of acute toxicity of radiotherapy.


Description:

The study will enroll 100 patients in current radiotherapy of the head and neck cancer with acute radiotoxic symptoms at least of G1. The patients will be randomized (by ticket) in two regimens 1:1.

Regimen A (control regimen): standard support treatment of adverse events of the radiotherapy.

Regimen B (acupuncture regimen): standard support treatment of adverse events of the radiotherapy and acupuncture.

Due to the disease and patients differences, treatment will be individualized. Used acupuncture points will be documented. The patients difficulties will be observed and their medication and will be recorded in the patient diary.

Possible skin toxicities wil be documented by the photography.

Before the randomization, all subjects will sign the voluntary informed consent. After the achievement of 50 enrolled subjects in any regimen, the enrollment will continue only to the other regimen.

Head and neck cancer therapy will include only curative and adjuvant radiotherapy.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date October 4, 2019
Est. primary completion date October 4, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Curative and adjuvant radiotherapy for head and neck tumors;

- PS 1-2;

- Patient collaboration in evaluation of the toxicity diary.

Exclusion Criteria:

- Palliative radiotherapy in the head and neck tumor;

- PS 3;

- Non-compliance of the patient.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Acupuncture
Schedule of the acupuncture: Acupuncture may be done ambulant or during hospitalisation . Acupuncture will be administered 1-3 times a week ( in case of severe toxicity and problems caused by the radiotherapy, it may continue also after the termination of the radiotherapy.) Acupuncture needles will be left for 5- 30 minutes, as per individual need of the patients. Acupuncture will be performed by a physician trained in acupuncture.
Drug:
Standard supportive therapy
Standard supportive therapy

Locations

Country Name City State
Czechia Masaryk Memorial Cancer Institute Brno

Sponsors (1)

Lead Sponsor Collaborator
Masaryk Memorial Cancer Institute

Country where clinical trial is conducted

Czechia, 

References & Publications (2)

Braga FP, Lemos Junior CA, Alves FA, Migliari DA. Acupuncture for the prevention of radiation-induced xerostomia in patients with head and neck cancer. Braz Oral Res. 2011 Mar-Apr;25(2):180-5. — View Citation

Meng Z, Garcia MK, Hu C, Chiang J, Chambers M, Rosenthal DI, Peng H, Zhang Y, Zhao Q, Zhao G, Liu L, Spelman A, Palmer JL, Wei Q, Cohen L. Randomized controlled trial of acupuncture for prevention of radiation-induced xerostomia among patients with nasopharyngeal carcinoma. Cancer. 2012 Jul 1;118(13):3337-44. doi: 10.1002/cncr.26550. Epub 2011 Nov 9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Management of acute toxicity of radiotherapy with acupuncture: Reducing the grade of acute toxicity in radiotherapy Reducing the grade of acute toxicity in radiotherapy. six months after the end of radiotherapy
Secondary Management of chronic toxicity of radiotherapy with acupuncture: Lower incidence of chronic toxicity of radiotherapy Lower incidence of chronic toxicity of radiotherapy. six months after the end of radiotherapy