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Postoperative Seroma Rate, Drainage Tube Removal Time, and Capsular Contracture RateRCT of PAI + PNCT07460297

Pseudomonas Aeruginosa Injection Combined With Polyvinylpyrrolidone-Iodine in Immediate Breast Reconstruction Surgery With Implants

A study testing Pseudomonas aeruginosa and Povidone-Iodine in people with Postoperative Seroma Rate, Drainage Tube Removal Time, and Capsular Contracture Rate and Seroma Following Procedure, run by Jianyi Li at 1 site in China.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Brief Summary This study hypothesizes that in immediate breast reconstruction following tumor resection, the application of inactivated Pseudomonas aeruginosa preparation (PAP) may reduce infection rates by decreasing postoperative drainage output and shortening drainage tube removal time. Read more about this study

Who is it for?
Ages 18 years and older, women only
What is being tested?
Pseudomonas aeruginosa and Povidone-Iodine
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
100 participants
Where
1 siteChina
Study dates
16 Apr 2025to 10 Jun 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18 and above
  • Female
  • Preoperative pathological confirmation of invasive breast cancer or ductal carcinoma in situ
  • Clinical T1 and T2 (maximum tumor diameter ≤5 cm)
  • Clinically negative axillary lymph nodes (clinical examination and ultrasound suggest negative axillary lymph nodes; fine needle aspiration is negative for suspected axillary lymph node abnormalities)
  • No clinical or radiological evidence of distant metastasis
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  • Patients undergoing skin-sparing mastectomy or breast-conserving surgery - BMI < 35
  • Patients without lactational apoptosis or with mild breast apoptosis
  • Implant volume < 500 milliliters (11) Able and willing to sign the informed consent form (ICF)

Who cannot join

  • Breast patients with moderate to severe breast development, or patients who require subcutaneous mastectomy using Wise mode or other breast lift methods
  • Body mass index >=35
  • Patients who underwent symmetrical breast surgery immediately or later on the unaffected side
  • Patients with locally advanced breast cancer receiving neoadjuvant therapy
  • Patients who are currently participating in other clinical trials, which may have an impact on participation in this trial
  • Neoadjuvant therapy has been completed, and there is a clear indication for adjuvant radiotherapy after surgery
Show all 10Show fewer
  • History of previous breast cancer (patients with ipsilateral recurrence after breast-conserving surgery)
  • Pregnant and lactating women
  • Smoking history
  • History of previous diabetes mellitus

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site
  • Liaoning Cancer Hospital and Institute

    Shenyang, Liaoning, 110000

Other trials in China

About this study

Official title: Pseudomonas Aeruginosa Injection Combined With Polyvinylpyrrolidone-Iodine in Immediate Breast Reconstruction Surgery With Implants:a Randomized Controlled Trial

Brief Summary

This study hypothesizes that in immediate breast reconstruction following tumor resection, the application of inactivated Pseudomonas aeruginosa preparation (PAP) may reduce infection rates by decreasing postoperative drainage output and shortening drainage tube removal time. Additionally, the local aseptic inflammation induced by PAP may promote fibrous capsule formation around the implant, shorten postoperative shaping time, and improve patients' quality of life and satisfaction. To test this hypothesis, the investigators designed a study to evaluate the efficacy of PAP compared with PI/TAB irrigation alone. Primary endpoints include drainage tube removal time and capsular contracture rate (assessed by Baker grade). Secondary endpoints include infection rate, total drainage volume, and postoperative BREAST-Q scores. Different concentrations of PAP will also be evaluated to determine the optimal therapeutic concentration.

Read more

Detailed Description

Postoperative infection rates in breast implant procedures range from 1% to 35%. Infection necessitates antibiotic treatment, may lead to unnecessary reoperations, and contributes to patient dissatisfaction. Inflammation and infection around the implant can promote biofilm formation, leading to capsular contracture (CC) following breast implant surgery. In patients undergoing breast reconstruction after tumor resection, postoperative infection may also delay adjuvant cancer treatment. Consequently, various antimicrobial irrigation solutions are routinely employed in immediate breast reconstruction after cosmetic surgery or tumor resection to reduce infection and CC rates, including 10% povidone-iodine (PI) and triple antibiotic solutions.

PI irrigation was first introduced by Burkhardt et al. in the 1980s for cosmetic breast surgery, followed by the development of a broader-spectrum triple antibiotic solution (TAB) by Adams et al. In 2000, the FDA prohibited the use of PI with breast implants due to concerns regarding higher contracture rates and potential degradation of silicone implants. Subsequent research by Adams et al. led to the development of a PI-free irrigation solution (TAB), which demonstrated comparable efficacy, albeit with slightly reduced coverage against Gram-negative bacteria. In August 2017, based on accumulated long-term data, the FDA lifted the restriction on PI use with implants, permitting its application for bacterial/biofilm mitigation and antimicrobial prophylaxis. Subsequent studies comparing the antimicrobial efficacy of PI and TAB have yielded mixed results, and a meta-analysis found no significant difference in CC rates between the two irrigation methods. However, the FDA withdrew bacitracin injections in 2020 due to safety concerns. As a result, standardization of antimicrobial irrigation solutions for implant-based immediate breast reconstruction remains lacking.

Notably, immediate reconstruction following tumor resection differs fundamentally from cosmetic surgery. For instance, the 14-point plan for cosmetic breast surgery recommends avoiding drainage tubes, a practice often unfeasible in immediate reconstruction, where two drainage tubes are typically placed for 4-7 days postoperatively. Breast surgeons aim to minimize drainage tube duration owing to the increased risk of surgical site infection (SSI). In immediate reconstruction, capsule formation time is prolonged compared with augmentation surgery, potentially leading to implant displacement and contracture.

PAP, derived from an inactivated PA-MSHA strain, has been shown by Long et al. to reduce postoperative drainage and shorten drainage tube removal time. PAP may also promote fibrous capsule formation, thereby reducing infection rates and improving patients' quality of life.

Read the detailed description

Postoperative infection rates in breast implant cases range from 1% to 35%. Infection requires antibiotic treatment, leads to unnecessary reoperations, and results in dissatisfaction. Inflammation and infection around the implant can cause biofilm formation, leading to capsular contracture (CC) after breast implant surgery. Postoperative infection may also delay adjuvant cancer treatment for patients undergoing breast reconstruction after tumor resection. Therefore, various antimicrobial irrigation solutions are commonly used in immediate breast reconstruction after cosmetic surgery or tumor resection to reduce infection and CC rates, such as 10% povidone-iodine (PI) and triple antibiotic solution.PI irrigation was proposed by Burkhardt et al. in the 1980s and used in cosmetic breast surgery, followed by the development of a broader-spectrum triple antibiotic solution (Betadine triple, BT) by Adams et al. Unfortunately, the FDA banned the use of PI with breast implants in 2000 due to reports of higher contraction rates and potential degradation of silicone implants. After further research, Adams et al. designed a PI-free irrigation solution (TAB) that was also effective, though with slightly lower coverage of Gram-negative bacteria.In August 2017, the FDA lifted the restriction on PI use with implants based on long-term data, allowing PI to be used for bacterial/biofilm mitigation and antimicrobial prophylaxis. Subsequent studies compared the antimicrobial efficacy of PI and TAB, with mixed results. A meta-analysis found no significant difference in CC rates between PI and TAB irrigation. However, the FDA withdrew bacitracin injections in 2020 due to safety concerns. As a result, there is still a lack of standardization in the choice of antimicrobial solutions for implant irrigation in immediate breast reconstruction surgery.

On the other hand, immediate reconstruction after tumor resection has different principles from cosmetic surgery, such as avoiding drainage tubes in the 14-point plan for breast cosmetic surgery. This is often not feasible in immediate reconstruction, where two drainage tubes are typically placed for 4-7 days postoperatively. Breast surgeons aim to minimize drainage tube time due to increased SSI risk. In immediate reconstruction, the capsule formation time is longer than in augmentation surgery, leading to potential implant displacement and contracture. PAP, prepared from an inactivated PA-MSHA strain, was shown to reduce drainage and shorten tube removal time by Long et al.. PAP may promote fibrous capsule formation, reducing infection rates and improving patient quality of life.

Being tested
Pseudomonas aeruginosa, Povidone-Iodine

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pseudomonas aeruginosaDrug

    Using two to six vials of PAP(Inactivated Pseudomonas aeruginosa injection) preparation combined with 100ml of iodophor to soak the implant and irrigate the surgical cavity.

  • Povidone-IodineDrug

    100ml povidone-iodin

Study groups in NCT07460297
Study groupRoleWhat they receive
PAP+PI groupExperimentalUsing two to six vials of PAP preparation combined with 100ml of iodophor to soak the implant and irrigate the surgical cavity
Receives: Drug: Pseudomonas aeruginosa; Drug: Povidone-Iodine
PI groupPlacebo comparatorUsing 100ml of iodophor only to soak the implant and irrigate the surgical cavity
Receives: Drug: Povidone-Iodine

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. seroma rate

    postoperative seroma rate

    Measured: Within 30 days post-surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Mar 2026
  2. Study start16 Apr 2025
  3. Primary completion10 Jan 2028 (estimated)
  4. Study completion10 Jun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Care provider, Outcomes assessor
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07460297
Sponsor's protocol ID
lnszl
Acronym
RCT of PAI + P
Status last verified
Mar 2026
First submitted
15 Apr 2025
Last updated
10 Mar 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Zhao M, Fang T, Jiang H, Li J. A randomized controlled trial: application of inactivated Pseudomonas aeruginosa preparation in nipple-sparing mastectomy with immediate prosthetic reconstruction for breast cancer. Gland Surg. 2026 Jul 31;15(7):189. doi: 10.21037/gs-2026-1-0135. Epub 2026 Jul 23.

    PubMed 42591819

Questions about this trial

What is this clinical trial studying?

A study testing Pseudomonas aeruginosa and Povidone-Iodine in people with Postoperative Seroma Rate, Drainage Tube Removal Time, and Capsular Contracture Rate and Seroma Following Procedure, run by Jianyi Li at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 10 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

seroma rate (time frame: Within 30 days post-surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07460297, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Mar 2026.

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