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Clinical Trials/KCT0001669
KCT0001669
Recruiting
未知

Feasibility of acupuncture treatment for symptoms after breast cancer surgery: a prospective case series

Kyung Hee University Oriental Medical Center0 sites10 target enrollmentTBD
ConditionsNot Applicable

Overview

Phase
未知
Intervention
Not specified
Conditions
Not Applicable
Sponsor
Kyung Hee University Oriental Medical Center
Enrollment
10
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
Female

Investigators

Sponsor
Kyung Hee University Oriental Medical Center

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients after breast cancer surgery and chemotherapy or radiotherapy at least 1 months before the participation
  • 2\. Women aged from 32 yrs to 64 yrs
  • 3\. Patients with at least 1 symptom below and severity of over 4 in 0 to 10 Numeric Rating Scale
  • 3\-1 Arthralgia after the treatment with Aromatase inhibitors
  • 3\-2 Hot flush or Sweating after the treatment with Anti\-estrogen agents
  • 3\-3 Insomnia
  • 3\-4 Sexual dysfunction (Vaginal dryness or Dyspareunia)
  • 3\-5 Pain after mastectomy
  • 4\. Patients who visits hospital on an outpatient basis regularly for additional treatments and monitoring after breast cancer surgery and chemotherapy or radiotherapy
  • 5\. Patients who would agree with the participation of this study and sign written informed consent

Exclusion Criteria

  • 1\. Those who have diseases or conditions below
  • 1\-1 Recurrence of tumor or having other primary cancer
  • 1\-2 Uncontrolled acute and chronic diseases
  • 1\-3 Uncontrolled current mental disorders including panic disorder, acute episode of mania, delusion, hallucination etc.
  • 1\-4 Having fear against acupuncture
  • 1\-5 Having above symptoms and diagnosed with specific diseases which introduce those symptoms before breast cancer surgery
  • 2\. Women who is pregnant, breast feeding or planning pregnancy
  • 3\. Anyone who does not have appropriate ability to answer questionnaires or has difficulty in visiting our clinical trial center
  • 4\. Anyone who is expected not to be appropriate to participate in this study judged by research personnel

Outcomes

Primary Outcomes

Not specified

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