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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00065234
Other study ID # R21AT001065-01A1
Secondary ID ChiangJ
Status Terminated
Phase Phase 2
First received July 18, 2003
Last updated March 27, 2017
Start date September 2003
Est. completion date May 2006

Study information

Verified date March 2017
Source National Center for Complementary and Integrative Health (NCCIH)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if acupuncture is effective in preventing prolonged postoperative paralysis of the gastrointestinal tract among patients undergoing colostomy/ileostomy closure.


Recruitment information / eligibility

Status Terminated
Enrollment 100
Est. completion date May 2006
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Previous surgical cancer treatment with ileostomy/colostomy, now scheduled for closure

- Hospital admission must be same day as surgery

Exclusion Criteria:

- Incapacitating disease

- Concurrent herbal or laxative use

- Use of Heparin or Coumadin

- Upper or lower extremity deformities

- Chronic constipation prior to cancer diagnosis

- History of cerebrovascular accident or spinal cord injury

- Chronic pain that has been treated with any form of major opioid or weak opioids (=/> 30mg/24 hours)

- Pacemaker or metal implants

- Concurrent alternative medicine/herbal use

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Acupuncture


Locations

Country Name City State
United States MD Anderson Cancer Center Houston Texas

Sponsors (1)

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

Country where clinical trial is conducted

United States, 

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