Using a 10% benzoyl peroxide acne wash on the shoulder before arthroscopic rotator cuff repair
Official title: Investigating Whether Preoperative Use of Acne Face Wash for Cleansing the Face, Neck, and Chest Helps Reduce the Contamination Rate of Cutibacterium Acnes in Arthroscopic Rotator Cuff Repair Surgery
Run by National Taiwan University Hospital · NCT07239349 · Data updated 2026-11-12
This trial tests whether washing the shoulder with a 10% benzoyl peroxide acne cleanser before arthroscopic rotator cuff repair reduces contamination by Cutibacterium acnes in patients with rotator cuff tears.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | National Taiwan University Hospital Academic / other |
| Locations | 1 site (Taipei) |
| Status | Recruiting |
| Started | November 18, 2025 |
| Main results expected | November 18, 2026 |
| Study ends | November 18, 2027 |
| Registry record updated | November 20, 2025 |
| Trial ID | NCT07239349 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with a rotator cuff tear who are scheduled for arthroscopic rotator cuff repair and who have no history of shoulder fracture, no prior shoulder surgeries, and no tattoos on the shoulder.
✕Probably not a fit
Patients with prior shoulder surgery, a history of shoulder fracture, or tattoos on the shoulder are excluded and therefore unlikely to receive benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, randomized trial that assigns patients undergoing arthroscopic rotator cuff repair to preoperative skin preparation with a 10% benzoyl peroxide (BPO) acne cleanser versus standard preparation. The study uses random allocation (random number table) and collects intraoperative cultures to measure contamination rates by Cutibacterium acnes from skin, surgical sites, or suture material. The goal is to compare the proportion of positive cultures between groups to determine whether preoperative BPO lowers contamination in rotator cuff procedures. Results are intended to inform preoperative preparation practices for shoulder arthroscopy.
Why it matters
Potential benefit: If successful, this simple preoperative wash could lower the rate of Cutibacterium acnes contamination during rotator cuff repairs and reduce related postoperative infections or complications.
How similar studies have gone: Previous studies in shoulder arthroplasty have shown that preoperative benzoyl peroxide can reduce C. acnes skin burden and lower joint or suture contamination, but strong evidence specifically for rotator cuff surgery is still limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * rotator cuff tear * scheduled for arthroscopic rotator cuff repair surgery Exclusion Criteria: * history of shoulder fracture * previous shoulder surgeries * tatoo on the shoulder
Where it's running
-
National Taiwan University Hospital
Taipei, Taiwan Recruiting
Study contacts
- Study coordinator: Chih-Kai Hong, M.D.
- Email: yayahong@gmail.com
- Phone: +886972651028
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Attention-shift exercise program for rotator cuff–related shoulder pain
This will test whether doing shoulder exercises while also performing attention-shifting movements reduces pain and improves function for people with rotator cuff-related shoulder pain.
-
Lok™ suture anchors: safety and performance
This will test whether Move‑Up's lok™ suture anchors are safe and help adults with rotator cuff or labrum injuries who need shoulder repair surgery.
-
FiberLocker® augmentation for rotator cuff repair
This study will test whether adding the FiberLocker® System (SpeedPatch® PET plus FiberLocker® Instrument) to arthroscopic repair improves healing and shoulder function in adults 30–70 with full-thickness rotator cuff tears of at least 2 cm.
-
Rotator cuff repair with SINEFIX vs a comparator device in adults with small tears
This study tests whether using the SINEFIX implant during rotator cuff repair helps adults with small tears heal and relieve pain.
-
Follow-up on the Integrity Implant System for shoulder rotator cuff tears
This study is testing whether the Integrity Implant System can help people with rotator cuff tears heal better and avoid re-injury.
-
Pitch-Patch Rotator Cuff Augmentation: Post-Market Follow-Up
This study follows patients who received the Pitch-Patch to reinforce partially repairable rotator cuff tears to see how well it performs and stays safe over the long term.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.