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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01849224
Other study ID # NCCNCS-13-723
Secondary ID
Status Recruiting
Phase Phase 3
First received May 6, 2013
Last updated July 15, 2013
Start date May 2013
Est. completion date December 2015

Study information

Verified date July 2013
Source National Cancer Center, Korea
Contact Myong Cheol Lim, MD, PhD
Phone +82-31-920-1760
Email gynlim@gmail.com
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary outcome is the change in lower extremity edema-related symptoms. Secondary outcomes include the compliance rate of management guidelines for lower extremity edema, the performance rate for pelvic and lower extremity exercise.


Recruitment information / eligibility

Status Recruiting
Enrollment 148
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- More than 18 years of age

- Patients who underwent pelvic lymphadenectomy

- Patients with suspicious pelvic cancer who finished active treatments such as chemotherapy, radiotherapy or surgery. The interval between the time of randomization and the end of the treatment should be more than 2 weeks.

- The patient is able to understand the study and is willing to give written informed consent to the study

- patient with edema-related symptoms such as leg heaviness, distension, tightness, pain, limited movement, or weakness etc.

Exclusion Criteria:

- Severe systemic diseases causing peripheral edema, including renal disease

- Severe or uncontrolled cardiopulmonary disease, including implantable device such as a pacemaker

- Acute superficial or deep vein thrombosis

- Previous major surgery for lower extremities, including metallic surgical implant

- Local infection in the lower extremities

- Auto-immunological disorders or vasculitis

- Use of systemic corticosteroids

- Pregnant or currently breastfeeding

- Alcohol or drug abuse

- Uncontrolled diabetes

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Pelvic and lower extremity exercise


Locations

Country Name City State
Korea, Republic of Myong Cheol Lim Goyang-si Gyeonggi-do

Sponsors (1)

Lead Sponsor Collaborator
National Cancer Center, Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in lower extremity edema-related symptoms after pelvic and lower extremities exercise 1 year after randomization No
Secondary the compliance rate of management guidelines for lower extremity edema, the performance rate for pelvic and lower extremity exercise 1 year after randomization No
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