Low Anterior Resection Syndrome, Rectal Cancer
Conditions
Keywords
PTNS, rectal cancer, low anterior resection syndrome
Brief summary
The study aims to evaluate the efficacy of percutaneous tibial nerve stimulation (PTNS) associated with conservative therapy (arm A) for the treatment of low anterior resection syndrome (LARS) compared with only conservative therapy (arm B). The secondary aims are the evaluation of the following parameters: * Effect of PTNS on manometric parameters * Effect of PTNS on quality of life * Effect of PTNS on the severity of fecal incontinence and / or obstructed defecation * Safety of PTNS
Detailed description
The study is a prospective randomized clinical trial that compares two treatments in patients with LARS: Arm A: PTNS + conservative treatment (based on predominant symptom) Arm B: only conservative treatment The study is divided into two phases: 1. PRETREATMENT PHASE The patients with LARS score ≥ 21 after anterior resection of the rectum with sphincter-saving surgery for rectal cancer, will be submitted during the first visit of the study to : * Collection of personal data * Collection of medical records * Collection of data relating to the intervention of anterior resection of the rectum * Verification of the criteria for inclusion / exclusion * Collection of informed consent * Administration of the questionnaires European Organisation for Research and Treatment of Cancer - Quality of Life Questionnaire Cancer 30 (EORTC QLQ-C30), European Organisation for Research and Treatment of Cancer - Quality of Life Questionnaire Colorectal 38 (EORTC QLQ-CR38), Faecal incontinence severity index (FISI); Fecal incontinence quality of life questionnaire (FIQL), Obstructed defaecation syndrome (ODS) score questionnaire and Constipation-related quality of life questionnaire (CRQoL) * Endoanal ultrasound * Anorectal manometry 2. PHASE OF TREATMENT During the treatment phase, data related to the treatment and any treatment related-complications will be recorded on a special form Bowel function and quality of life will be assessed using the same questionnaires at the end of treatment. Even anorectal manometry will be repeated at the end of treatment. It is expected to enroll approximately 12 patients.
Interventions
DEVICEPTNS
Sponsors
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Patients with LARS score ≥ 21 after anterior resection of the rectum with sphincter-saving surgery for rectal cancer; * Age\> 18 years; * Obtaining informed consent.
Exclusion criteria
* Patients carrying ostomy; * Patients with clinical or radiological evidence of local or distant tumor recurrence; * Patients suffering from neurological disorders; * Patients with Inflammatory Bowel Disease (IBD); * Patients who have a pacemaker or defibrillator; * Patients taking antiplatelet agents or anticoagulants; * Patients unable to follow the procedures of the Protocol or to provide informed consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| LARS score | 67 weeks | The primary end point is the evaluation of the results of the two interventions in functional terms, by comparing the LARS score calculated first at the end and after 12 months of treatment, according to the following classification: * No LARS: a score between 0 and 20 * LARS mild: score between 21:29 * LARS severe: a score between 30 and 42 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| EORTC QLQ-C30 | 67 weeks | Secondary objectives will be evaluated by the change of the questionnaires EORTC QLQ-C30 performed before and after treatment |
| FISI | 67 weeks | Secondary objectives will be evaluated by the change of the questionnaires FISI examinations performed before and after treatment. |
| FIQL | 67 weeks | Secondary objectives will be evaluated by the change of the questionnaires FIQL performed before and after treatment. |
| EORTC QLQ-CR38 | 67 weeks | Secondary objectives will be evaluated by the change of the questionnaires EORTC QLQ-CR38 performed before and after treatment. |
| CRQoL | 67 weeks | Secondary objectives will be evaluated by the change of the questionnaires CRQoL performed before and after treatment. |
| functional outcome | 67 weeks | Functional outcome will be evaluated comparing manometric examinations performed before and after treatment. |
| morbidity | 67 weeks | registration of complications after each therapy session |
| ODS SCORE | 67 weeks | Secondary objectives will be evaluated by the change of the questionnaires ODS score performed before and after treatment. |
Countries
Italy
Contacts
Primary ContactDajana Cuicchi, MD PhD
Outcome results
None listed