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.
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
- Conditions the study is for
- Postoperative Seroma Rate, Drainage Tube Removal Time, and Capsular Contracture Rate, Seroma Following Procedure
- 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
Show all 9Show fewer
- 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.
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.
- Conditions
- Postoperative Seroma Rate, Drainage Tube Removal Time, and Capsular Contracture Rate, Seroma Following Procedure
- 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 group | Role | What they receive |
|---|---|---|
| PAP+PI group | Experimental | Using 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 group | Placebo comparator | Using 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.
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.
- First posted10 Mar 2026
- Study start16 Apr 2025
- Primary completion10 Jan 2028 (estimated)
- Study completion10 Jun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Postoperative Seroma Rate, Drainage Tube Removal Time, and Capsular Contracture RateStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Jianyi Li
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Jianyi Li, Shengjing Hospital
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
Study at a glance
From the registry record, last updated by the sponsor on 10 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pseudomonas Aeruginosa Injection Combined With Polyvinylpyrrolidone-Iodine in Immediate Breast Reconstruction Surgery With Implants:a Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT07460297
- Acronym / sponsor ID
- RCT of PAI + P / lnszl
- Conditions
- Postoperative Seroma Rate, Drainage Tube Removal Time, and Capsular Contracture Rate, Seroma Following Procedure
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Jianyi LiUniversity, hospital or other
- Study start
- 16 Apr 2025 (actual)
- Primary completion
- 10 Jan 2028 (estimated)
- Study completion
- 10 Jun 2028 (estimated)
- First posted
- 10 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| PAP+PI group | Experimental | Drug: Pseudomonas aeruginosa, Drug: Povidone-IodineUsing two to six vials of PAP preparation combined with 100ml of iodophor to soak the implant and irrigate the surgical cavity |
| PI group | Placebo comparator | Drug: Povidone-IodineUsing 100ml of iodophor only to soak the implant and irrigate the surgical cavity |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (9 listed)
- 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)
Key exclusion criteria (10 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Pseudomonas aeruginosaUsing 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. | Drug | PAP+PI group |
| Povidone-Iodine100ml povidone-iodin | Drug | PAP+PI group, PI group |
Primary outcome
seroma rate
Time frame: Within 30 days post-surgery
postoperative seroma rate
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Mar 2026.
- Derived from this study: PubMed 42591819Zhao 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.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.