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Administrative reasons
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Open label pilot study assessing FMT to treat fecal incontinence in women 50 years of age and older.
Fecal incontinence, also known as accidental bowel leakage, is a common condition that is an immense burden to older women, caregivers, and the health care system. The overall goal of this study is to gather pilot data in order to conduct a future randomized controlled trial (RCT) for a novel treatment for fecal incontinence in older women utilizing fecal microbial transplantation (FMT). The investigator's hypothesis is that infusion of intestinal microbiota from healthy donors to older women with fecal incontinence will increase microbial diversity, reduce symptom severity, and improve quality of life. This study is a single arm, open-label clinical trial of FMT for the treatment of fecal incontinence refractory to conservative management. The investigators will measure the impact of FMT on change in symptom severity and quality of life and stool microbial diversity at 4 and 12 weeks after FMT.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| FMT Administration | Experimental | This is a single arm study in which all eligible participants will receive FMT. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| fecal microbial transplantation (FMT) | Biological | Fecal microbial transplantation (FMT) is the infusion of intestinal microbiota from healthy donors. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Subjects That Show Significant Improvement at 4 Weeks After FMT, and Will be Maintained at 12 Weeks, Relative to Baseline Using the St. Mark's Vaizey Score, a Measure of Fecal Incontinence Severity. | The St Marsk's Viazy score is a validated patient-reported instrument used to measure fecal incontinence severity. Score ranges from 0-24 with a decrease in the score representing an improvement. A subject has clinical improvement if they have demonstrated a sustained decrease of 4-5 points between the 4-week and 12-week measurements. | 84 days |
| Count of Participants With Adverse Events. | Frequency of adverse events, serious adverse events, and adverse events of special interest (including allergic reaction and gastrointestinal symptoms). | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Subjects That Have an Improved Quality of Life at 4 and 12 Weeks, Measured by the FIQL Scale. | The FIQL is a valid and reliable 29-item questionnaire designed to evaluate the impact of FI on four aspects (domains) of patients' quality of life: lifestyle; coping behavior; depression or self-perception; and level of embarrassment. Domain scores range from 1-4 (higher scores indicating better quality of life). An improvement in the score of 1 (one) within each domain would indicate an improvement in the quality of life. |
| Measure | Description | Time Frame |
|---|---|---|
| Count of Participants That Demonstrate Engraftment Following Fecal Microbial Transplantation. | Concentration of microbiota at baseline vs concentration of microbiota at 4 weeks. | 28 days |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Uduak U Andy, MD | University of Pennsylvania | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital of the University of Pennsylvania | Philadelphia | Pennsylvania | 19104 | United States |
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10 Subjects were enrolled. 2 subjects dropped out prior to administration of the investigational product. 8 subjects were treated with the investigational product.
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| ID | Title | Description |
|---|---|---|
| FG000 | FMT Administration | This is a single arm study in which all eligible participants will receive FMT. Fecal microbial transplantation (FMT) is the infusion of intestinal microbiota from healthy donors. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | FMT Administration | This is a single arm study in which all eligible participants will receive FMT. fecal microbial transplantation (FMT): Fecal microbial transplantation (FMT) is the infusion of intestinal microbiota from healthy donors. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Subjects That Show Significant Improvement at 4 Weeks After FMT, and Will be Maintained at 12 Weeks, Relative to Baseline Using the St. Mark's Vaizey Score, a Measure of Fecal Incontinence Severity. | The St Marsk's Viazy score is a validated patient-reported instrument used to measure fecal incontinence severity. Score ranges from 0-24 with a decrease in the score representing an improvement. A subject has clinical improvement if they have demonstrated a sustained decrease of 4-5 points between the 4-week and 12-week measurements. | Posted | Count of Participants | Participants | 84 days |
|
6 months
Frequency of adverse events, serious adverse events, and adverse events of special interest (including allergic reactions and gastrointestinal symptoms)
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | FMT Administration | This is a single arm study in which all eligible participants will receive FMT. Fecal microbial transplantation (FMT) is the infusion of intestinal microbiota from healthy donors. |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Abdominal Bloating | Gastrointestinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Regulatory Lead | University of Pennsylvania | 215-662-4484 | psom-ind-ide@pobox.upenn.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Sep 19, 2022 | Feb 21, 2024 | Prot_SAP_000.pdf |
| ICF | No | No | Yes | Informed Consent Form | Oct 28, 2022 | Feb 21, 2024 | ICF_001.pdf |
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| ID | Term |
|---|---|
| D005242 | Fecal Incontinence |
| ID | Term |
|---|---|
| D012002 | Rectal Diseases |
| D007410 | Intestinal Diseases |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
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| 84 days |
| Count of Participants That Demonstrate Microbial Engraftment Following Fecal Microbial Transplantation and Demonstrate Clinical Improvement. | Concentration of Microbiota present at baseline vs at week 4 in subjects that demonstrate a significant improvement at 4 weeks after FMT, relative to baseline using the St. Mark's Vaizey score. | 28 days |
| Participants |
| No |
|
| Age, Continuous | Mean | Standard Deviation | years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Units | Counts |
|---|---|
| Participants |
|
|
| Primary | Count of Participants With Adverse Events. | Frequency of adverse events, serious adverse events, and adverse events of special interest (including allergic reaction and gastrointestinal symptoms). | Posted | Count of Participants | Participants | 6 months |
|
|
|
| Secondary | Number of Subjects That Have an Improved Quality of Life at 4 and 12 Weeks, Measured by the FIQL Scale. | The FIQL is a valid and reliable 29-item questionnaire designed to evaluate the impact of FI on four aspects (domains) of patients' quality of life: lifestyle; coping behavior; depression or self-perception; and level of embarrassment. Domain scores range from 1-4 (higher scores indicating better quality of life). An improvement in the score of 1 (one) within each domain would indicate an improvement in the quality of life. | Posted | Count of Participants | Participants | 84 days |
|
|
|
| Secondary | Count of Participants That Demonstrate Microbial Engraftment Following Fecal Microbial Transplantation and Demonstrate Clinical Improvement. | Concentration of Microbiota present at baseline vs at week 4 in subjects that demonstrate a significant improvement at 4 weeks after FMT, relative to baseline using the St. Mark's Vaizey score. | Posted | Count of Participants | Participants | 28 days |
|
|
|
| Other Pre-specified | Count of Participants That Demonstrate Engraftment Following Fecal Microbial Transplantation. | Concentration of microbiota at baseline vs concentration of microbiota at 4 weeks. | Posted | Count of Participants | Participants | 28 days |
|
|
|
| 0 |
| 8 |
| 0 |
| 8 |
| 6 |
| 8 |
| Abdominal Pain | Gastrointestinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
| Belching | Gastrointestinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
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| Constipation | Gastrointestinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
| Diarrhea | Gastrointestinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
| Flatulence | Gastrointestinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
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| Nausea | Gastrointestinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
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| Rectal Hemorrhage | Gastrointestinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
| Fatigue | General disorders | CTCAE Version 5.0 | Non-systematic Assessment |
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| General Disorder and administrative site conditions - Other - nasal irritation | General disorders | CTCAE Version 5.0 | Non-systematic Assessment |
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| General disorders and administration site conditions - Other - nostril pain | General disorders | CTCAE Version 5.0 | Non-systematic Assessment |
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| Dizziness | Nervous system disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
| Laryngeal Inflammation | Respiratory, thoracic and mediastinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
| Rhinorrhea | Respiratory, thoracic and mediastinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
| Sore Throat | Respiratory, thoracic and mediastinal disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
| Epistaxis | Vascular disorders | CTCAE Version 5.0 | Non-systematic Assessment |
|
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