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Secondary Bilateral Sacral Nerve Stimulation in Overactive Bladder Patients (NEUROBIL)

Primary Purpose

Bladder Hyperactivity

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Device: INTERSTIM II
Sponsored by
University Hospital, Rouen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bladder Hyperactivity focused on measuring relapse after an initial clinical response

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients implanted with Sacral Neuro Modulation for idiopathic OAB with initial efficacy of at least 3 months following by a failure despite optimization of the stimulation (minimum 3)
  • OAB evaluated by voiding diary: number of frequency ≥ 8/24 h or urgencies ≥ 3 during 3 days, with or without urge incontinence.
  • Age between 18 and 80 years.

Exclusion Criteria:

  • Psychiatric or neurologic disabilities on neurologic evaluation.
  • Bladder lithiasis or tumor (cystoscopy or ultrasonography).
  • Treatment by drugs that could interfere with the OAB syndromes.
  • Pelvic floor exercises should have been interrupted 1 month before.
  • No planned surgery on bladder or urinary neurologic tract.
  • Diuresis > 3 liters per 24 hours.
  • Negative test at the end of screening period.

Sites / Locations

  • UH Caen
  • UH Grenoble
  • GHICL Lille Saint Philibert
  • Lille University Hospital
  • Hospices civiles de Lyon
  • AP-HM
  • UH Nantes
  • UH Nîmes
  • AP-HP Pitié Salpetrière
  • AP-HP Tenon
  • UH Rouen
  • UH Toulouse

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Alone controlateral stimulation

2 sides-stimulation

Arm Description

Device: INTERSTIM II Stimulator II activated Stimulator I not activated Measure of efficacy on bladder hyperactivity

Device: INTERSTIM II Stimulator I and II activated Measure of efficacy on bladder hyperactivity

Outcomes

Primary Outcome Measures

Success of Test Period
A successful response is defined as greater than 50% improvement in at least one relevant voiding parameters, with bilateral stimulation versus baseline without stimulation. Relevant voiding diary parameters are: urgency number, frequency, urge incontinence number. These criteria are commonly used in the studies on sacral neuromodulation.

Secondary Outcome Measures

Effect of alone controlateral stimulation
Effect of alone controlateral stimulation on : urgency, frequency, urge incontinence.
Effect of alone controlateral stimulation
Effect of alone controlateral stimulation on : Quality of Life (QoL) scores
Effect of alone controlateral stimulation
Effect of alone controlateral stimulation on : VAS pain scale
Effect of alone controlateral stimulation
Effect of alone controlateral stimulation on : Adverse events.
Effect of alone controlateral stimulation
Prognostic factors of success will be evaluated concerning age, sex, urodynamic parameters, period of time of symptoms before first implant, period of time between first implant and controlateral/bilateral stimulation, complete failure or a partial failure of efficiency of initial stimulator.

Full Information

First Posted
July 4, 2013
Last Updated
June 26, 2020
Sponsor
University Hospital, Rouen
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1. Study Identification

Unique Protocol Identification Number
NCT01960270
Brief Title
Secondary Bilateral Sacral Nerve Stimulation in Overactive Bladder Patients
Acronym
NEUROBIL
Official Title
Secondary Bilateral or Controlateral Sacral Nerve Stimulation in Overactive Bladder Patients With Unilateral Stimulation Failure - Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
November 12, 2013 (Actual)
Primary Completion Date
May 2, 2018 (Actual)
Study Completion Date
May 2, 2018 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Unilateral sacral neuromodulation (SNM) has emerged as a valuable treatment for patient with low urinary tract dysfunction when failure or bad tolerance to anticholinergic treatment for overactive bladder. However, in the medium or long term, some patients failed to benefit from unilateral stimulation (unilateral neuromodulation). A contralateral stimulation could be tested then implanted to restore the efficacy. An other option is to perform a bilateral stimulation of the sacral nerves that could lead to a summation effects better than unilateral stimulation. Therefore, if a unilateral sacral nerve stimulation fails, a contralateral or a bilateral test should be considered.
Detailed Description
Sacral neuromodulation (SNM) is a treatment in non neurogenic (idiopathic) patients with overactivity of the bladder (OAB) symptoms, refractory to conservative treatment. After selection of patients with positive stimulation test (PNE test), the success rate of stimulation implant is approximatively 70% (40 to 80%). Unilateral versus bilateral initial implantation was retrospectively compared by Pham et al. with respectively 58 and 77% success rate. Wound infection and complication rate were similar. However the limitation of bilateral stimulation is an increased cost for the health care system, augmented duration of the procedure, possible morbidity. Therefore initial implantation in the first step of the treatment is unilateral in current practice. However, after a period of time, a secondary failure may happen, either a complete failure with return to initial symptom or a partial failure with a decrease of the efficacy that may impact on quality of life. However, a non clinical evident effect could have a summation effect if a contralateral stimulator was implanted, and possibly better than contralateral alone. Research have shown in a small study on 15 patients that a selected group of patients appear to benefit from bilateral stimulation test (PNE test) after failure of unilateral S3 stimulation. A successful response was observed in 4/11 (36%) OAB patients. Bilateral stimulation induced a higher clinical response than stimulation of a controlateral lead alone in voiding parameters. In the patients who showed a successful response to PNE test, 3 were implanted bilaterally with more than 50% improvement for 2 of them at one year follow-up, and 41% improvement for the third. No painful stimulation or side effects were reported with chronic bilateral stimulation. In one study, a lead migration was suspected in 3/15 patients and was the cause of failure. Therefore the proposed study will use systematically a tined lead electrode that avoid lead migration. According to these preliminary data, test stimulation with a contralateral lead might be considered in secondary unsuccessful patient and evaluated. Further investigation is necessary to determine in a larger cohort the result of contralateral alone or bilateral stimulator implantation. There is no established guidelines in secondary unsuccessful patients, therefore contralateral stimulation is used in clinical practice according to patient and practitioner opinion. This protocol is presented as a standard clinical practice evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Hyperactivity
Keywords
relapse after an initial clinical response

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Alone controlateral stimulation
Arm Type
Experimental
Arm Description
Device: INTERSTIM II Stimulator II activated Stimulator I not activated Measure of efficacy on bladder hyperactivity
Arm Title
2 sides-stimulation
Arm Type
Experimental
Arm Description
Device: INTERSTIM II Stimulator I and II activated Measure of efficacy on bladder hyperactivity
Intervention Type
Device
Intervention Name(s)
Device: INTERSTIM II
Intervention Description
A second stimulator is implanted on controlateral site
Primary Outcome Measure Information:
Title
Success of Test Period
Description
A successful response is defined as greater than 50% improvement in at least one relevant voiding parameters, with bilateral stimulation versus baseline without stimulation. Relevant voiding diary parameters are: urgency number, frequency, urge incontinence number. These criteria are commonly used in the studies on sacral neuromodulation.
Time Frame
Day 0
Secondary Outcome Measure Information:
Title
Effect of alone controlateral stimulation
Description
Effect of alone controlateral stimulation on : urgency, frequency, urge incontinence.
Time Frame
Day 30 and day 60
Title
Effect of alone controlateral stimulation
Description
Effect of alone controlateral stimulation on : Quality of Life (QoL) scores
Time Frame
Day 30 and day 60
Title
Effect of alone controlateral stimulation
Description
Effect of alone controlateral stimulation on : VAS pain scale
Time Frame
Day 30 and day 60
Title
Effect of alone controlateral stimulation
Description
Effect of alone controlateral stimulation on : Adverse events.
Time Frame
Day 30 and day 60
Title
Effect of alone controlateral stimulation
Description
Prognostic factors of success will be evaluated concerning age, sex, urodynamic parameters, period of time of symptoms before first implant, period of time between first implant and controlateral/bilateral stimulation, complete failure or a partial failure of efficiency of initial stimulator.
Time Frame
Day 30 and day 60

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients implanted with Sacral Neuro Modulation for idiopathic OAB with initial efficacy of at least 3 months following by a failure despite optimization of the stimulation (minimum 3) OAB evaluated by voiding diary: number of frequency ≥ 8/24 h or urgencies ≥ 3 during 3 days, with or without urge incontinence. Age between 18 and 80 years. Exclusion Criteria: Psychiatric or neurologic disabilities on neurologic evaluation. Bladder lithiasis or tumor (cystoscopy or ultrasonography). Treatment by drugs that could interfere with the OAB syndromes. Pelvic floor exercises should have been interrupted 1 month before. No planned surgery on bladder or urinary neurologic tract. Diuresis > 3 liters per 24 hours. Negative test at the end of screening period.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe GRISE, Pr
Organizational Affiliation
UH Rouen
Official's Role
Principal Investigator
Facility Information:
Facility Name
UH Caen
City
Caen
Country
France
Facility Name
UH Grenoble
City
Grenoble
Country
France
Facility Name
GHICL Lille Saint Philibert
City
Lille
Country
France
Facility Name
Lille University Hospital
City
Lille
Country
France
Facility Name
Hospices civiles de Lyon
City
Lyon
Country
France
Facility Name
AP-HM
City
Marseille
Country
France
Facility Name
UH Nantes
City
Nantes
Country
France
Facility Name
UH Nîmes
City
Nîmes
Country
France
Facility Name
AP-HP Pitié Salpetrière
City
Paris
Country
France
Facility Name
AP-HP Tenon
City
Paris
Country
France
Facility Name
UH Rouen
City
Rouen
ZIP/Postal Code
76031
Country
France
Facility Name
UH Toulouse
City
Toulouse
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
17869298
Citation
van Kerrebroeck PE, van Voskuilen AC, Heesakkers JP, Lycklama a Nijholt AA, Siegel S, Jonas U, Fowler CJ, Fall M, Gajewski JB, Hassouna MM, Cappellano F, Elhilali MM, Milam DF, Das AK, Dijkema HE, van den Hombergh U. Results of sacral neuromodulation therapy for urinary voiding dysfunction: outcomes of a prospective, worldwide clinical study. J Urol. 2007 Nov;178(5):2029-34. doi: 10.1016/j.juro.2007.07.032. Epub 2007 Sep 17.
Results Reference
result
PubMed Identifier
18551562
Citation
Pham K, Guralnick ML, O'Connor RC. Unilateral versus bilateral stage I neuromodulator lead placement for the treatment of refractory voiding dysfunction. Neurourol Urodyn. 2008;27(8):779-81. doi: 10.1002/nau.20577.
Results Reference
result
PubMed Identifier
21247601
Citation
Marcelissen TA, Leong RK, Serroyen J, van Kerrebroeck PE, De Wachter SG. The use of bilateral sacral nerve stimulation in patients with loss of unilateral treatment efficacy. J Urol. 2011 Mar;185(3):976-80. doi: 10.1016/j.juro.2010.10.065. Epub 2011 Jan 19.
Results Reference
result

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Secondary Bilateral Sacral Nerve Stimulation in Overactive Bladder Patients

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