Ethosuximide to Treat IBS

Irritable Bowel Syndrome Clinical Trial

— IBSET  

Official title:

Evaluation of the Efficacy and Tolerance of Ethosuximide in the Treatment of Abdominal Pain Associated With Irritable Bowel Syndrome

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02973542
• Other study ID #: CHU-289
• Secondary ID: 2016-002110-42
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: April 30, 2018
• Est. completion date: May 2023

Study information

• Verified date: April 2022
• Source: University Hospital, Clermont-Ferrand
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Abdominal pain remains the most deleterious symptom for patients with irritable bowel syndrome (IBS) and is causing a significant alteration of their quality of life. The visceral hypersensitivity seems to be one of the key mechanisms that could explain the abdominal pain in these patients. Current treatments, mainly symptomatic, are of limited effectiveness, especially in terms of relief of abdominal pain. The study will aim to evaluate the effectiveness of ethosuximide on abdominal pain in patients with IBS, its tolerance and its impact on patient quality of life, severity of symptoms related to IBS and the use of analgesics / antispasmodic / regulators transit.

Description:

The irritable bowel syndrome (IBS) is characterized by a combination of discomfort and / or abdominal pain and bowel habits in the absence of identifiable organic pathology. This condition is extremely common because it is the first cause of consultation in gastroenterology and would cover 10-15% of the French. This chronic condition, although functional, impact significantly on the quality of life of patients and causes considerable health spending, making it a major public health problem. Especially as the currently used treatments are of limited effectiveness.

Among the pathophysiological mechanisms involved in IBS, visceral hypersensitivity (VHS) seems to be a major factor causing pain in patients. VHS involves sensitization of colonic nerve fibers, resulting in an increase of neuronal excitability. In several animal models of chronic pain, this hyperexcitability was related to a change in the expression or activity of ion channels, including calcium channel Cav3.2.

Investigators especially shown the involvement of Cav3.2 channels in visceral pain in an animal model of VHS. Furthermore, overexpression of these channels at the peripheral level (dorsal root ganglion innervating the colon) has been demonstrated in this animal model and pharmacological blockade, including ethosuximide, prevented the development of the VHS. Note that Cav3.2 channels have been widely demonstrated as involved in nociceptive phenomena in various animal models of chronic pain and that by blocking their ethosuximide induce an analgesic effect in these models.

Finally, we have recently demonstrated the involvement of Cav3.2 channel in patients with IBS, in a clinical case-control study. The Cav3.2 channels were overexpressed in the colonic mucosa of patients with IBS compared to asymptomatic controls.

The Cav3.2 channels are therefore a potential pharmacological target and ethosuximide a promising therapy to effectively treat the abdominal pain associated with IBS.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 162
• Est. completion date: May 2023
• Est. primary completion date: April 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age = 18 years,

• Man,

• Women, Negative pregnancy test and effective contraception,

• IBS defined by the Rome criteria IV

• During the previous seven days the inclusion visit, average NRS pain = 4,

• IBS Treatment stable for 1 month

• Patients affiliated to the French Social Security,

• Patients with the informed consent were obtained.

Exclusion Criteria:

• Breastfeeding

• Diabetic patients

• Known renal or hepatic impairment,

• Significant liver function abnormalities (transaminases> 3N, cholestasis) and renal (MDRD <60 ml / min)

• Addiction to alcohol and / or drugs,

• AEDs taken (epilepsy or chronic pain)

• chronic pain of greater intensity than that related to IBS,

• Allergy succinimides (ethosuximide, methsuximide, phensuximide)

• History or current severe depression (hospitalization, long-term antidepressant treatment)

• Psychotic disorders,

• Patients exclusion period, or total exceeded authorized allowances

• Patients undergoing a measure of legal protection (trusteeship, guardianship ...).

Related Conditions & MeSH terms

• Irritable Bowel Syndrome
• Syndrome

Intervention

Drug:
• Ethosuximide
The study will aim to evaluate the effectiveness of ethosuximide on abdominal pain in patients with IBS, its tolerance and its impact on patient quality of life, severity of symptoms related to IBS and the use of analgesics / antispasmodic / regulators transit.

Other:
• Placebo
The study will aim to evaluate the effectiveness of ethosuximide on abdominal pain in patients with IBS, its tolerance and its impact on patient quality of life, severity of symptoms related to IBS and the use of analgesics / antispasmodic / regulators transit.

Locations

Country	Name	City	State
France	CHU Clermont-Ferrand	Clermont-Ferrand

Sponsors (2)

Lead Sponsor	Collaborator
University Hospital, Clermont-Ferrand	SFETD (Socièté Française d'Etude et de Traitement de la Douleur)

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	30% reduction in abdominal pain		through study completion, an average of 12 weeks.
Primary	Score of 4 or 5 on the SGA scale		through study completion, an average of 12 weeks.
Secondary	Monthly assessment of abdominal pain		at 1 month
Secondary	Monthly assessment of score of Bristol scale		at 1 month
Secondary	Monthly evaluation of GIQLI questionnaire		at 1 month
Secondary	Monthly evaluation of EQ-5D questionnaire		at 1 month
Secondary	Monthly evaluation of IBS-SSS questionnaire		at 1 month
Secondary	Monthly evaluation of SGA scale.		at 1 month
Secondary	Monthly evaluation of the use of analgesics		at 1 month
Secondary	Monthly evaluation of the use of antispasmodic		at 1 month
Secondary	Monthly evaluation of the use of regulators transit.		at 1 month
Secondary	Monthly evaluation of medical response rate		at 1 month
Secondary	Monthly evaluation of stop work related to IBS.		at 1 month
Secondary	Evaluation of the tolerance of ethosuximide throughout the study.		at 1 month
Secondary	Evaluation of the discontinuation rate study because of adverse events throughout the study		at 1 month