Predicting Treatment Outcomes in Refractory Constipation Through Brain Connectivity Evaluation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-45
SponsorXijing Hospital of Digestive Diseases

About this trial

The goal of this observational study is to identify the characteristics of brain functional connectivity in refractory constipation and fluoxetine-sensitive patients. The main questions it aims to answer are:

* Investigating the alterations in brain functional connectivity in patients with refractory constipation and fluoxetine-sensitive patients * Assessing the predictive value of brain functional connectivity regarding the efficacy of fluoxetine and standard protocol treatments for constipation.

Participants will receive:

* Standard physiological and psychological assessments of constipation * BOLD-fMRI tests * Standard protocol and fluoxetine treatment

If there is a comparison group: Researchers will compare:

Refractory group/Fluoxetine sensitive group to see the specific brain alterations.

Eligibility criteria

Qualifiers

18≤ age ≤ 45 years old

Right-handed

Patients diagnosed as functional constipation according to the Rome IV criteria

Informed consent of patients

Disqualifiers

Complicated with gastrointestinal organic disease or significant functional abnormalities (tuberculosis, polyps, Crohn's disease, tumors, congenital megacolon, pelvic floor muscle relaxation, abnormal colonic transit test, etc.)

Long-term intense exercise (continuous exercise for more than 8 hours per week, such as marathon runners or triathletes)

No history of chronic pain, no recent major trauma

Drug abuse or tobacco dependence (half a pack or more per day)

Trial design

Treatments tested in this trial

  • BOLD-fMRI
  • Regular treatment of functional constipation
  • fluoxetine

Treatment groups

150 Participants
are divided into 4 treatment groups