Efficacy of Pregabalin for Patients With Irritable Bowel Syndrome

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorBeijing Tiantan Hospital

About this trial

To explore the efficacy of pregabalin for patients with irritable bowel syndrome (IBS).

Eligibility criteria

Qualifiers

Age range: 18-70 years old;

According to the Rome IV diagnostic criteria for IBS, the screening result is positive;

Mild to moderate IBS patients assessed based on the IBS-SSS.

Disqualifiers

Concurrent gastrointestinal conditions presenting with symptoms potentially overlapping with those of IBS, significant medical comorbidities;

Severe mental disorders associated with marked personality disturbances, active suicidal thoughts or any self harm episodes within the preceding 12 months;

Current or intended pregnancy or lactation;

Cognitive impairment;

Trial design

Treatments tested in this trial

  • The pregabalin group
  • Routine Treatment

Treatment groups

258 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Beijing Tiantan Hospital

Lead sponsor

Hengshui People's Hospital

Collaborator

Hebei Medical University Third Hospital

Collaborator

Beijing Jianjia Rehabilitation Hospital

Collaborator