Effect of Amitriptyline and Trifluoperazine on Patients With Functional Dyspepsia
Launched by MD. MOKTADIRUL HOQUE SHUVO · Jun 4, 2025
Trial Information
Current as of July 23, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how effective two medications, amitriptyline and trifluoperazine, are in treating symptoms of functional dyspepsia, which is a condition that causes discomfort or pain in the upper abdomen. The trial aims to see if these medications can help improve symptoms compared to standard treatment. Researchers will also keep track of any side effects participants may experience while taking these medications to ensure they are safe.
To participate in this trial, you need to be at least 18 years old and have been diagnosed with functional dyspepsia. You should not have certain health issues, such as serious liver problems or a history of specific cancers, and you should not be pregnant or breastfeeding. If you join, you will take either amitriptyline or trifluoperazine along with standard treatment for 8 weeks, and then you will continue with only the standard treatment for an additional 4 weeks. Throughout the trial, you will visit the hospital every four weeks to discuss your symptoms and any side effects you may have experienced.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 18 years or more
- • Patients with FD diagnosed according to ROME IV criteria
- • Patients who are willing to sign informed written consent
- Exclusion Criteria:
- • Structural lesion in endoscopy and positive CLO test
- • Patients scoring 1 or 2 on the 5-point Likert scale for all four dyspepsia symptoms
- • History of malignancy, liver and biliary tract disease, diabetes mellitus, chronic kidney disease
- • Major medical and psychiatric disorders
- • Previous history gastrointestinal surgery
- • Any patient with ongoing treatment with antidepressants or antipsychotics
- • Any history of hypersensitivity, adverse effect, or ineffectiveness with amitriptyline or trifluoperazine
- • Patients for whom Amitriptyline and Trifluoperazine are contraindicated
- • Elderly patients\> 60 years
- • Pregnancy and breastfeeding
About Md. Moktadirul Hoque Shuvo
Dr. Moktadirul Hoque Shuvo is a dedicated clinical trial sponsor with a strong commitment to advancing medical research and improving patient outcomes. With extensive experience in clinical trial management and a focus on innovative therapeutic solutions, Dr. Shuvo leads initiatives that prioritize ethical practices, rigorous scientific methodologies, and collaboration with healthcare professionals. His leadership is characterized by a passion for enhancing healthcare through evidence-based research, ensuring that trials are conducted with the highest standards of quality and integrity.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Dhaka, , Bangladesh
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported