The Effect of Arista on Post-Operative Bleeding and Wound Drainage Following Mastectomy
Completed · Not applicable
Conditions studied: Seroma
In brief
Study aim was to evaluate topical MPH on the risk of post-mastectomy seroma formation as measured by total drain output and total drain days.
Key facts
- Study ID
- NCT03647930
- Run by
- Memorial Health University Medical Center
- People needed
- 50
- Starts
- 2012-05-15
- Expected to finish
- 2015-03-06
- Last updated by the study team
- 2018-08-27
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Age greater than or equal to 18 years
- Undergoing simple mastectomy with or without sentinel lymph nodes biopsy OR modified radical mastectomy for the treatment of breast cancer
You may not qualify if…
- Undergoing partial mastectomy
- Sentinel lymph node biopsy requiring conversion to axillary lymph node dissection
- Immediate reconstructive surgery
- Systemic anticoagulation
- Choosing not to participate in the study
Where it is running
- Memorial Health University Medical Center — Savannah, Georgia, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.