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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00067691
Other study ID # R21AT001029-01
Secondary ID
Status Completed
Phase N/A
First received August 25, 2003
Last updated August 16, 2006
Start date November 2001
Est. completion date November 2003

Study information

Verified date August 2006
Source National Center for Complementary and Integrative Health (NCCIH)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether acupuncture is effective in relieving shortness of breath among breast and lung cancer patients.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date November 2003
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Diagnosis of local or metastatic breast or lung cancer

- Shortness of breath with onset after cancer diagnosis

- Life expectancy of at least 4 weeks

Exclusion Criteria:

- Prior acupuncture

- Other conditions suspected of causing shortness of breath, such as congestive heart failure, sarcoid disease, pneumonia, or obesity

- No chest wall deformity

- Neuromuscular disorders

- Pulmonary vascular disease

- Anemia

- Uncontrolled pain or infection

- Heart valve dysfunction

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Acupuncture


Locations

Country Name City State
United States Memorial Sloan-Kettering Institute for Cancer Research New York New York

Sponsors (2)

Lead Sponsor Collaborator
National Center for Complementary and Integrative Health (NCCIH) National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

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