Impact of showering on infection rates and quality of life after breast reconstruction
Effect of Drain Care on Infection Rate and Quality of Life in Implant-Based Breast Reconstruction.
This study is testing if showering with drain tubes after breast reconstruction surgery affects infection rates and how patients feel during recovery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | Female |
| Sponsor | University of Missouri-Columbia Academic / other |
| Locations | 1 site (Columbia, Missouri) |
| Trial ID | NCT05846438 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates whether showering with surgical drain tubes in place after breast reconstruction surgery increases the risk of infection and affects patients' quality of life. Participants will be randomized into two groups: one group will shower daily after 48 hours post-surgery, while the other will follow the standard care of waiting until drains are removed. The study aims to provide insights into postoperative care practices and their implications for patient outcomes.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 undergoing breast surgery with tissue expander placement and drains.
Not a fit: Patients with existing wounds or previous infections related to implant devices may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved postoperative care practices that enhance patient quality of life without increasing infection risks.
How similar studies have performed: While there is limited research specifically on showering with drains in place, similar studies have explored postoperative care practices, indicating potential for meaningful insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * undergoing breast surgery with placement of tissue expander and drains, acceptance of protocol and procedures, age \> 18 Exclusion Criteria: * no existing wounds, previous infections related to implant device if delayed, refusal by patient
Where this trial is running
Columbia, Missouri
- University of Missouri — Columbia, Missouri, United States (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.