Acupuncture |
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Clinical Trial: Acupuncture for Neck and Shoulder Pain Following Neck Surgery in Cancer Patients
This study is currently recruiting patients.
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Purpose
The purpose of this study is to determine whether acupuncture therapy reduces neck and shoulder pain in patients who have undergone neck dissection surgery for the treatment of head and neck cancer.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Head and Neck Neoplasms Neck Pain Shoulder Pain | Procedure: Acupuncture | Phase III |
MedlinePlus related topics: Head and Neck Cancer; Neck Disorders and Injuries; Pain
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Acupuncture for Pain and Dysfunction Following Neck Dissection: A Randomized, Controlled Phase III Trial
Expected Total Enrollment: 60
Study start: December 2003
Neck dissection is a common procedure for the treatment of head and neck cancer; unfortunately, patients often suffer from neck and shoulder pain following the procedure. Standard care for neck dissection pain consists of physical therapy exercises and the use of nonsteroidal anti-inflammatory drugs. Studies suggest that acupuncture may relieve pain caused by neck dissection. This study will determine the effectiveness of acupuncture therapy in relieving the pain of neck dissection patients.
Participants in this study will be randomly assigned to receive either acupuncture treatments once a week for 4 weeks or standard care. Self-report questionnaires and scales that measure pain, level of functioning, and overall quality of life will be used to assess participants. Participants assigned to the standard care group will be offered four treatments of acupuncture at the end of the study.
Eligibility
Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- Neck dissection for head and/or neck cancer at least 3 months prior to study entry
- Moderate to severe pain and/or dysfunction in the neck and/or shoulders due to neck dissection
- Radiotherapy treatment at least 3 months prior to study entry
Exclusion Criteria:
- Acupuncture 6 weeks prior to study entry
Location and Contact Information
Cheryl Co 212-639-8610
New York
Memorial Sloan-Kettering Cancer Center, New York, New York, 10021, United States; Recruiting
Barrie Cassileth, PhD, Sub-Investigator
More Information
Record last reviewed: March 2005
Last Updated: March 24, 2005
Record first received: August 25, 2004
ClinicalTrials.gov Identifier: NCT00090337
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 8, 2005

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