Fistula RepairERGNCT06930079
Endoscopic Injection of Autologous, Activated and Emulsified Fat in Chronic Fistulas of the Gastrointestinal Tract and Pelvic Organs
An observational study of Fistula Repair, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS at 1 site in Italy.
Trial summary
Fistulas are defined as pathologic communications between two epithelialized surfaces and represent a complex nosologic entity that often exposes the patient to life-threatening or disabling sequelae. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Fistula Repair
- Type of treatment
- Injection or infusion
- How many people
- 43 participants
- Where
- 1 siteItaly
- Study dates
- 20 Mar 2025to 20 Dec 2027
- Phase
- Observational
- 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
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: patients with chronic fistula of the pelvic organs and/or the gastrointestinal tract of any type, being symptomatic and/or impacting the quality of life
Who may be able to join
- Male or female patients having a diagnosis of chronic fistula (diagnosis at least 3 months before the enrollment) of the pelvic organs and/or the gastrointestinal tract of any type, being symptomatic and/or impacting the quality of life.
- Age of at least 18 years.
- Able to comply with study requirements and understand and sign the Informed Consent Form.
Who cannot join
- Impaired hemostasis or any contraindication to perform endoscopy or liposuction.
- Any contraindication to perform deep sedation or general anesthesia.
- Woman being pregnant at the time of the procedure.
- Malignancy in active treatment.
- Any health issue that might put the patient at risk if the treatment is performed is judged by the investigator.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Italy1 site, 1 recruiting
- Recruiting
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Rome, 00168
Ivo Boskoski, 0630155701, ivo.boskoski@policlinicogemelli.it
About this study
Official title: Observational, Prospective Single-center Study on the Results of Endoscopic Injection of Autologous, Activated and Emulsified Fat in Chronic Fistulas of the Gastrointestinal Tract and Pelvic Organs
Fistulas are defined as pathologic communications between two epithelialized surfaces and represent a complex nosologic entity that often exposes the patient to life-threatening or disabling sequelae. Their etiology can vary widely (spontaneous, iatrogenic, post-surgical perforation, anastomotic dehiscence, inflammatory process) and their treatment is complex, sometimes unresolved, and often requires a multidisciplinary approach. The chronicity of digestive and pelvic organ fistulas (e.g., vagino-vesical fistulas) is related to tissue repair mechanisms, which are delayed and subverted in favor of fibrotic and inflammatory processes. In these cases, the wound healing cascade stops at the inflammatory phase and does not result in the proliferation phase. The transition depends on changing levels of cytokines and growth factors. In the persistence of the inflammatory phase, polymorphonucleates and macrophages are active, phagocytosing and releasing enzymes that also damage healthy tissue. In this context, the anti-inflammatory, angiogenic, antiapoptotic, and tissue regenerative effects of adipose tissue-derived stromal or stem cells (ADSCs) could play a decisive role. In fact, ADSCs exhibit immunosuppressive properties on the proliferation of T cells, B lymphocytes, dendritic cells, and natural killer cells and modulate inflammation by implanting a regenerative niche with appropriate paracrine communication and subsequent tissue regeneration. "Fat grafting" has a wide range of application: it started with plastic surgery and regenerative medicine, then in orthopedics, maxillofacial surgery, and vascular surgery. Since 2019, a new procedure using processed fat grafting for the treatment of chronic fistulas of the gastrointestinal tract and pelvic organs has been initiated at the Agostino Gemelli IRCCS University Polyclinic Foundation and has become "standard of care," with good results. The procedure is quick, safe, minimally invasive and cost-effective. Subcutaneous fat, immediately after harvesting from the same patient, is mechanically stimulated with oscillatory movements, then injected under endoscopic vision directly onto the orifice of the fistula. When the fat is centrifuged, it stimulates the activation of various mesenchymal stemness-related genes, such as Sox2, Nanog and Oct4. The increase in mRNAs is tens to hundreds of times and is accompanied by a pronounced increase in the expression of the anti-inflammatory protein TSG6 and suppression of TNFalpha, normally expressed by adipose tissue.
The objective of the study is to treat chronic fistula of the gastrointestinal tract and pelvic organs of any type, symptomatic and/or impacting quality of life, in whom all other treatments (medical, endoscopic, or surgical) have failed or are not candidates.
Our primary endpoint is to evaluate the efficacy of the injection of autologous activated adipose tissue injection in these cases. Secondary endpoints evaluate the changes in patients' quality of life and the long-term efficacy of the activated fat injection.
- Conditions
- Fistula Repair
- Keywords
- fistula
- Medical subject headings
- Fistula
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| chronic fistulas of the GI tract or pelvic organs | Autologous activated fat tissue injection |
What is being measured
The primary outcome is the main question the study is designed to answer.
number of participants with fistula resolution at 6 months after the procedure.
Endoscopic and/or radiological evaluation
Measured: 6 months
Secondary outcomes (2)
number of participants with fistula resolution at 2 months after the procedure.
Endoscopic evaluation
Measured: 2 months
Quality of life measure before and after the procedure
Short Form Health Survey 36 (SF-36) test will be administered at screening visit, then at 6 and 12 months after the procedure; 0 is the worst possible outcome and 100 is the best possible outcome
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Apr 2025
- Study start20 Mar 2025
- Primary completion31 Mar 2027 (estimated)
- Study completion20 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Fistula RepairStudies of the same condition, open and under way.
- More trials run by Fondazione Policlinico Universitario Agostino Gemelli IRCCSThe sponsor's other registered studies.
- 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
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 43 participants (estimated)
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, BOSKOSKI IVO, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06930079
- Sponsor's protocol ID
- 7097
- Acronym
- ERG
- Status last verified
- Feb 2025
- First submitted
- 20 Mar 2025
- Last updated
- 18 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Observational, Prospective Single-center Study on the Results of Endoscopic Injection of Autologous, Activated and Emulsified Fat in Chronic Fistulas of the Gastrointestinal Tract and Pelvic Organs
- ClinicalTrials.gov ID
- NCT06930079
- Acronym / sponsor ID
- ERG / 7097
- Conditions
- Fistula Repair
- Keywords
- fistula
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 43 participants (estimated)
- Lead sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCSUniversity, hospital or other
- Study start
- 20 Mar 2025 (actual)
- Primary completion
- 31 Mar 2027 (estimated)
- Study completion
- 20 Dec 2027 (estimated)
- First posted
- 16 Apr 2025 (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.
Fistulas are defined as pathologic communications between two epithelialized surfaces and represent a complex nosologic entity that often exposes the patient to life-threatening or disabling sequelae. Their etiology can vary widely (spontaneous, iatrogenic, post-surgical perforation, anastomotic dehiscence, inflammatory process) and their treatment is complex, sometimes unresolved, and often requires a multidisciplinary approach. The chronicity of digestive and pelvic organ fistulas (e.g., vagino-vesical fistulas) is related to tissue repair mechanisms, which are delayed and subverted in favor of fibrotic and inflammatory processes. In these cases, the wound healing cascade stops at the inflammatory phase and does not result in the proliferation phase. The transition depends on changing levels of cytokines and growth factors. In the persistence of the inflammatory phase, polymorphonucleates and macrophages are active, phagocytosing and releasing enzymes that also damage healthy tissue. In this context, the anti-inflammatory, angiogenic, antiapoptotic, and tissue regenerative effects of adipose tissue-derived stromal or stem cells (ADSCs) could play a decisive role. In fact, ADSCs exhibit immunosuppressive properties on the proliferation of T cells, B lymphocytes, dendritic cells, and natural killer cells and modulate inflammation by implanting a regenerative niche with appropriate paracrine communication and subsequent tissue regeneration. "Fat grafting" has a wide range of application: it started with plastic surgery and regenerative medicine, then in orthopedics, maxillofacial surgery, and vascular surgery. Since 2019, a new procedure using processed fat grafting for the treatment of chronic fistulas of the gastrointestinal tract and pelvic organs has been initiated at the Agostino Gemelli IRCCS University Polyclinic Foundation and has become "standard of care," with good results. The procedure is quick, safe, minimally invasive and cost-effective. Subcutaneous fat, immediately after harvesting from the same patient, is mechanically stimulated with oscillatory movements, then injected under endoscopic vision directly onto the orifice of the fistula. When the fat is centrifuged, it stimulates the activation of various mesenchymal stemness-related genes, such as Sox2, Nanog and Oct4. The increase in mRNAs is tens to hundreds of times and is accompanied by a pronounced increase in the expression of the anti-inflammatory protein TSG6 and suppression of TNFalpha, normally expressed by adipose tissue.
The objective of the study is to treat chronic fistula of the gastrointestinal tract and pelvic organs of any type, symptomatic and/or impacting quality of life, in whom all other treatments (medical, endoscopic, or surgical) have failed or are not candidates.
Our primary endpoint is to evaluate the efficacy of the injection of autologous activated adipose tissue injection in these cases. Secondary endpoints evaluate the changes in patients' quality of life and the long-term efficacy of the activated fat injection.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| chronic fistulas of the GI tract or pelvic organs | – | –Autologous activated fat tissue injection |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- patients with chronic fistula of the pelvic organs and/or the gastrointestinal tract of any type, being symptomatic and/or impacting the quality of life
Key inclusion criteria (3 listed)
- Male or female patients having a diagnosis of chronic fistula (diagnosis at least 3 months before the enrollment) of the pelvic organs and/or the gastrointestinal tract of any type, being symptomatic and/or impacting the quality of life.
- Age of at least 18 years.
- Able to comply with study requirements and understand and sign the Informed Consent Form.
Key exclusion criteria (5 listed)
- Impaired hemostasis or any contraindication to perform endoscopy or liposuction.
- Any contraindication to perform deep sedation or general anesthesia.
- Woman being pregnant at the time of the procedure.
- Malignancy in active treatment.
- Any health issue that might put the patient at risk if the treatment is performed is judged by the investigator.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
number of participants with fistula resolution at 6 months after the procedure.
Time frame: 6 months
Endoscopic and/or radiological evaluation
2 secondary outcomes
number of participants with fistula resolution at 2 months after the procedure.
Time frame: 2 months
Quality of life measure before and after the procedure
Time frame: 12 months
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 18 Apr 2025.
- Individual participant dataSharing planned: No
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Fistula Repair, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS at 1 site in Italy.
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 3 inclusion and 5 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: looking for participants now, as of the sponsor's last update on 18 Apr 2025. 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 Italy. 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. 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?
Contact Ivo Boskoski (0630155701, ivo.boskoski@policlinicogemelli.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
number of participants with fistula resolution at 6 months after the procedure. (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 18 Apr 2025.