Post-Breast Procedure Pain Syndrome Study

Withdrawn before enrolling

Conditions studied: Breast, Mastectomy, Segmental

In brief

The purpose of this study is to better understand and characterize the pain that some patients experience after undergoing various breast surgeries, including breast biopsy, lumpectomy, mastectomy, mastectomy with reconstruction, cosmetic breast augmentation, and breast reduction.

Key facts

Study ID

NCT01114984

Run by

Cedars-Sinai Medical Center

People needed

0

Starts

2009-07-01

Expected to finish

2014-06-01

Last updated by the study team

2015-03-02

Who can join

Age: 18 and older, up to 80. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Patients scheduled to undergo one or more of the breast surgical procedures being studied for this project
• Willingness and ability to sign an informed consent document
• No allergies to anesthetic or analgesic medications
• Female,
• 18-80 years of age
• ASA class I-III adult

You may not qualify if…

• Patients with known allergy, hypersensitivity or contraindications to anesthetic or analgesic medications
• Patients with clinically-significant medical conditions, such as brain, heart, kidney, endocrine, or liver diseases, or history of chronic pain syndrome or neuropathy.
• Subjects with a history of alcohol or drug abuse within the past 3 months
• Subjects with a history of pain medication abuse
• Any other conditions or use of any medication which may interfere with the conduct of the study

Where it is running

• Cedars Sinai Medical Center — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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