CHU de Nantes
Nantes, 44000, France
NCT Number: NCT02748590
Efficacy of ulcerative colitis to induce remission in patients with moderate to severe active ulcerative colitis.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Nantes, 44000, France
Neuromodulation is a validated option for the treatment of fecal incontinence. Safety of this original approach has been confirmed by several studies. New indications for this minimally-invasive procedure are actually under evaluation particularly in the fields of irritable bowel syndrome and chronic constipation with promising results. Its mechanism of action remains partially unknown and the target of neuromodulation is not limited to the anal sphincter but the whole colonic motility seems to be influenced by this therapeutic approach. Moreover, recent experimental studies have shown that neuromodulation was able to reinforce the intestinal epithelial barrier involved in the pathophysiology of ulcerative colitis.
Subsequently, preliminary results in human have shown improvement of inflammation in patients suffering from inflammatory bowel diseases. In fact, despite recent improvement in medical therapies in inflammatory bowel diseases and particularly in ulcerative colitis, several patients are suffering from disabling chronic active disease. In those cases of refractory diseases, the only alternative treatment is a pan-proctocolectomy and ileal pouch surgery. This approach is a curative option, but leads to a significant morbidity and frequent functional disorders in the long-term follow-up (permanent stoma in 7 to 10% of the cases). Moreover, in limited distal disease (left colon and rectum) the surgical option seems to be unadapted and many patients remain symptomatic and suffer chronic active disease.
The aim of this study will be to assess in a prospective pilot study the efficacy of ulcerative colitis in inducing the remission of chronic active ulcerative colitis limited to the left side of the colon and improving the quality of life of the patients.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The neuromodulation will be carried out according to the usual protocol: Hospitalization for the establishment of percutaneous electrode in the operating room under general anesthesia with fluoroscopic control. The pacemaker startup will be performed within 12h after surgery
Time frame: 8 weeks
Clinical and endoscopic remission as measured by the Mayo score ≤ 2 points without any criteria> 1 point to week 8
Time frame: 16 weeks
Remission is defined by a Mayo score ≤ 1 point.
Time frame: 16 weeks
The response is defined as a decrease of at least 1 point in the item assessment by the physician and at least 1 point from the 3 other items with no increase in the other dimensions of the score.
Time frame: 16 weeks
The answer Clinic is defined as a decrease of at least 3 points in the score Clinic dimension compared to baseline.
Time frame: 16 weeks
Endoscopic response corresponds to a decrease of at least 1 point in the endoscopic score
Time frame: 16 weeks
Mucosal healing is defined by a score of Geboes less than or equal to 1 of the biopsy examination
Time frame: 16 weeks
Biological response is defined as a decrease of C-reactive protein
Time frame: 16 weeks
Biological response is defined as a decrease of fecal calprotectin.
Time frame: 16 weeks
The resolution is defined by bleeding Ulcerative Colitis Disease Activity Index sub-score 0
Time frame: 16 weeks
The resolution is defined by bleeding Ulcerative Colitis Disease Activity Index sub-score 0
Time frame: 16 weeks
Cessation of rectal bleeding is defined as rectal bleeding Ulcerative Colitis Disease Activity Index sub-score of 0
Time frame: 16 weeks
Absence or decreasing in immunosuppressive drugs during the follow-up
Time frame: 16 weeks
The need for steroid treatment at least once during the follow-up period
Time frame: 16 weeks
Tolerance of neuromodulation is stated by symptom specific scale
Time frame: 16 weeks
Quality of life is evaluated with The Short Form 36 scale
Time frame: 16 weeks
Bristol Stool Scale
Nantes University Hospital
Other
Evaluation of Sacral Neuromodulation (SNM) in the Treatment of Active Ulcerative Colitis
Acronym: PRIMICISTIM
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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