Secondary Bilateral Sacral Nerve Stimulation in Overactive Bladder Patients

NCT ID: NCT01960270

Last Updated: 2020-06-29

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-11-12
• Study Completion Date: 2018-05-02

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.

Conditions

Bladder Hyperactivity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Alone controlateral stimulation

Device: INTERSTIM II

• Stimulator II activated
• Stimulator I not activated
• Measure of efficacy on bladder hyperactivity

Group Type: EXPERIMENTAL

Device: INTERSTIM II

Intervention Type: DEVICE

A second stimulator is implanted on controlateral site

2 sides-stimulation

Device: INTERSTIM II

• Stimulator I and II activated
• Measure of efficacy on bladder hyperactivity

Group Type: EXPERIMENTAL

Device: INTERSTIM II

Intervention Type: DEVICE

A second stimulator is implanted on controlateral site

Interventions

Device: INTERSTIM II

A second stimulator is implanted on controlateral site

Intervention Type: DEVICE

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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Rouen

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Philippe GRISE, Pr

Role: PRINCIPAL_INVESTIGATOR

UH Rouen

Locations

UH Caen

Caen, , France

UH Grenoble

Grenoble, , France

GHICL Lille Saint Philibert

Lille, , France

Lille University Hospital

Lille, , France

Hospices civiles de Lyon

Lyon, , France

AP-HM

Marseille, , France

UH Nantes

Nantes, , France

UH Nîmes

Nîmes, , France

AP-HP Pitié Salpetrière

Paris, , France

AP-HP Tenon

Paris, , France

UH Rouen

Rouen, , France

UH Toulouse

Toulouse, , France

Countries

France

References

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.

Reference Type: RESULT

PMID: 17869298 (View on PubMed)

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.

Reference Type: RESULT

PMID: 18551562 (View on PubMed)

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.

Reference Type: RESULT

PMID: 21247601 (View on PubMed)

Other Identifiers

2013/003/HP

Identifier Type: -

Identifier Source: org_study_id