Efficacy of Sacral Nerve Modulation in Severe Refractory Constipation

The prevalence of constipation is 2-27% in Western countries. For patients failing medical treatment (laxatives, biofeedback), a surgical solution may be considered (subtotal colectomy). But results are variable and it puts them at risk of functional sequelae.

Sacral nerve modulation is a minimally invasive procedure compared with the standard surgical support (colectomy) and reversible, which consists in two stages. First, a 3-week temporary stimulation test allows verifying the efficacy of neuromodulation. If the test is positive, the stimulating electrode is definitely implanted. Risks related to the procedure (infection, pain) are much smaller than those associated with a conventional surgical support.

Non comparative studies conducted with 19 and 62 patients showed that 40-73% of implanted patients have an improvement of their constipation and could benefit of permanent implantation with good results in medium term.

The primary objective of the investigators study is to evaluate the short-term efficacy (percentage of responders at 2 months) of sacral nerve modulation in the treatment of severe chronic constipation.

This is a cross-over designed, double-blinded, French multicenter clinical trial, including two periods: 2 months of stimulation ON and 2 months of stimulation OFF. Between these two periods, a 15-days period of "wash-out" will be respected during which all patients will be in OFF mode (4.5 months in total). This period of 4.5 months will be extended by a follow-up period of 7 months during which all patients will be treated (stimulation ON).

If this trial showed efficiency of this procedure, patients with severe refractory constipation could benefit of a sacral nerve modulation test before considering a surgical treatment.

Inclusion criteria

• Age ≥ 18 years old
• Constipation defined by at least two of the following criteria :

• Frequency of 2 stools or less per week
• Severe outlet constipation, i.e. need to use digital extraction or enemas more than 25% of time
• Sensation of incomplete evacuation more than 25% of time
• Refractory constipation since at least 1 year to medical treatment (drug treatment and/or biofeedback) conducted in the centre (failure or intolerance to laxative osmotic treatments, stimulants, and prucalopride) for which surgery is discussed
• Patients supported in the centre for at least 3 months before inclusion
• Patients having social security system
• Patients having read and signed informed consent form

Exclusion criteria

• Constipation secondary to ano-rectal malformation, surgical sequel, colorectal or anal organic lesions, or pelvi-perineal static disorder indicated for surgical treatment
• Constipation secondary to neurological pathology and/or concomitant treatments intake (opiates, anticholinergic agents)
• Partial colectomy history
• Patients in whom implantation of stimulating electrode is impossible due to anatomical reasons (e.g. sacral agenesis)
• Pregnant female patients or with childbearing potential without adequate contraceptive barrier (oestrogen-progesterone contraceptives or intra-uterine device)
• Skin disease associated with a risk of infection - in the opinion of the investigator
• Patient with pacemaker or defibrillator
• Patient exposed to resonance magnetic imaging
• Psychiatric disease incompatible with use of the treatment - in the opinion of the investigator
• Patient misunderstanding oral and written French language
• Patient participating to another study
• Patients who don't complete the first diary without missing data (concerning items used to define the primary endpoint)