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Evaluation of Sacral Neuromodulation (SNM) in the Treatment of Active Ulcerative Colitis (PRIMICISTIM) (PRIMICISTIM)

Primary Purpose

Active Ulcerative Colitis

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
InterStim II Neurostimulator Model 3058
Sponsored by
Nantes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Active Ulcerative Colitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Active Ulcerative Colitis diagnosed on criteria Lennard Jones (31) for at least 1 year
  • > 18 yo
  • E1 - E2 disease or extended to transverse colon but not beyond the hepatic flexure (endoscopic pictures)
  • resistant to medical treatment: active after introduction for at least 8 weeks of maintenance treatment (immunosuppressive or anti-TNF)
  • Activity score >5 and endoscopic score >2
  • Absence of bacterial infection in progress (Clostridium difficile)
  • Affiliated with a social protection scheme and had signed an informed consent

Exclusion Criteria:

  • Severe forms requiring hospitalization an intravenous treatment or immediate surgery
  • infectious colitis or proctitis
  • Prednisone> 20 mg / d
  • Contraindications to the use of neuromodulator
  • Corticosteroid therapy by intravenous route
  • Pregnant women
  • Major Trust

Sites / Locations

  • CHU de Nantes

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Neuromodulation

Arm Description

Outcomes

Primary Outcome Measures

Efficacy of neuromodulation to induce remission at Week 8 in patients with moderate to severe active ulcerative colitis (Mayo score)
Clinical and endoscopic remission as measured by the Mayo score ≤ 2 points without any criteria> 1 point to week 8

Secondary Outcome Measures

Assess the Remission at Week 16 ( Mayo score)
Remission is defined by a Mayo score ≤ 1 point.
Assess the Response at Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
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.
Assess the clinical response at Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
The answer Clinic is defined as a decrease of at least 3 points in the score Clinic dimension compared to baseline.
Assess the endoscopic response at Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
Endoscopic response corresponds to a decrease of at least 1 point in the endoscopic score
Assess the histological response at Week 8 and Week 16 (Geboes Score)
Mucosal healing is defined by a score of Geboes less than or equal to 1 of the biopsy examination
Assess the biological response at Week 8 and Week 16 (C-reactive protein)
Biological response is defined as a decrease of C-reactive protein
Assess the biological response at Week 8 and Week 16 (Calprotectin)
Biological response is defined as a decrease of fecal calprotectin.
Evaluate the symptom's resolution at Week 3, Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
The resolution is defined by bleeding Ulcerative Colitis Disease Activity Index sub-score 0
Evaluate the urgencies cessation at Week 3, Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
The resolution is defined by bleeding Ulcerative Colitis Disease Activity Index sub-score 0
Evaluate the cessation of rectal bleeding at Week 8, Week 16
Cessation of rectal bleeding is defined as rectal bleeding Ulcerative Colitis Disease Activity Index sub-score of 0
Evaluate the immunosuppressive drugs at Week 8 and Week 16
Absence or decreasing in immunosuppressive drugs during the follow-up
Evaluate the need for steroids at Week 8 and Week 16
The need for steroid treatment at least once during the follow-up period
Evaluate the tolerance of neuromodulation in Ulcerative Colitis patients at Week 3, Week 8 and Week 16
Tolerance of neuromodulation is stated by symptom specific scale
Evaluate the quality of life of the patients at Week 8 and Week 16 (Scale The Short Form 36)
Quality of life is evaluated with The Short Form 36 scale
Assess abdominal discomfort for weeks at Week 8 and Week 16
Bristol Stool Scale

Full Information

First Posted
April 14, 2016
Last Updated
March 30, 2020
Sponsor
Nantes University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02748590
Brief Title
Evaluation of Sacral Neuromodulation (SNM) in the Treatment of Active Ulcerative Colitis (PRIMICISTIM)
Acronym
PRIMICISTIM
Official Title
Evaluation of Sacral Neuromodulation (SNM) in the Treatment of Active Ulcerative Colitis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
June 2016 (undefined)
Primary Completion Date
January 2020 (Actual)
Study Completion Date
January 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nantes University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Efficacy of ulcerative colitis to induce remission in patients with moderate to severe active ulcerative colitis.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Active Ulcerative Colitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Neuromodulation
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
InterStim II Neurostimulator Model 3058
Intervention Description
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
Primary Outcome Measure Information:
Title
Efficacy of neuromodulation to induce remission at Week 8 in patients with moderate to severe active ulcerative colitis (Mayo score)
Description
Clinical and endoscopic remission as measured by the Mayo score ≤ 2 points without any criteria> 1 point to week 8
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Assess the Remission at Week 16 ( Mayo score)
Description
Remission is defined by a Mayo score ≤ 1 point.
Time Frame
16 weeks
Title
Assess the Response at Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
Description
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
Title
Assess the clinical response at Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
Description
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
Title
Assess the endoscopic response at Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
Description
Endoscopic response corresponds to a decrease of at least 1 point in the endoscopic score
Time Frame
16 weeks
Title
Assess the histological response at Week 8 and Week 16 (Geboes Score)
Description
Mucosal healing is defined by a score of Geboes less than or equal to 1 of the biopsy examination
Time Frame
16 weeks
Title
Assess the biological response at Week 8 and Week 16 (C-reactive protein)
Description
Biological response is defined as a decrease of C-reactive protein
Time Frame
16 weeks
Title
Assess the biological response at Week 8 and Week 16 (Calprotectin)
Description
Biological response is defined as a decrease of fecal calprotectin.
Time Frame
16 weeks
Title
Evaluate the symptom's resolution at Week 3, Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
Description
The resolution is defined by bleeding Ulcerative Colitis Disease Activity Index sub-score 0
Time Frame
16 weeks
Title
Evaluate the urgencies cessation at Week 3, Week 8 and Week 16 (scale Ulcerative Colitis Disease Activity Index)
Description
The resolution is defined by bleeding Ulcerative Colitis Disease Activity Index sub-score 0
Time Frame
16 weeks
Title
Evaluate the cessation of rectal bleeding at Week 8, Week 16
Description
Cessation of rectal bleeding is defined as rectal bleeding Ulcerative Colitis Disease Activity Index sub-score of 0
Time Frame
16 weeks
Title
Evaluate the immunosuppressive drugs at Week 8 and Week 16
Description
Absence or decreasing in immunosuppressive drugs during the follow-up
Time Frame
16 weeks
Title
Evaluate the need for steroids at Week 8 and Week 16
Description
The need for steroid treatment at least once during the follow-up period
Time Frame
16 weeks
Title
Evaluate the tolerance of neuromodulation in Ulcerative Colitis patients at Week 3, Week 8 and Week 16
Description
Tolerance of neuromodulation is stated by symptom specific scale
Time Frame
16 weeks
Title
Evaluate the quality of life of the patients at Week 8 and Week 16 (Scale The Short Form 36)
Description
Quality of life is evaluated with The Short Form 36 scale
Time Frame
16 weeks
Title
Assess abdominal discomfort for weeks at Week 8 and Week 16
Description
Bristol Stool Scale
Time Frame
16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Active Ulcerative Colitis diagnosed on criteria Lennard Jones (31) for at least 1 year > 18 yo E1 - E2 disease or extended to transverse colon but not beyond the hepatic flexure (endoscopic pictures) resistant to medical treatment: active after introduction for at least 8 weeks of maintenance treatment (immunosuppressive or anti-TNF) Activity score >5 and endoscopic score >2 Absence of bacterial infection in progress (Clostridium difficile) Affiliated with a social protection scheme and had signed an informed consent Exclusion Criteria: Severe forms requiring hospitalization an intravenous treatment or immediate surgery infectious colitis or proctitis Prednisone> 20 mg / d Contraindications to the use of neuromodulator Corticosteroid therapy by intravenous route Pregnant women Major Trust
Facility Information:
Facility Name
CHU de Nantes
City
Nantes
ZIP/Postal Code
44000
Country
France

12. IPD Sharing Statement

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Evaluation of Sacral Neuromodulation (SNM) in the Treatment of Active Ulcerative Colitis (PRIMICISTIM)

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