Major Depression Clinical Trials

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Effect of Psychobiotics (Combined Lactobacillus Helveticus and Bifidobacterium Longus) With Standard Antidepressants in Treatment of Major Depressive Disorder.

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn whether adding psychobiotics (a combination of Lactobacillus helveticus and Bifidobacterium longum) to standard antidepressant treatment works better than antidepressants alone for adults with major depressive disorder. The study will also learn about the safety of taking these psychobiotics with antidepressants. The main questions it aims to answer are: 1. Does adding psychobiotics lower depression symptoms more than a placebo (a look-alike capsule with no active ingredients)? 2. Is it safe and well tolerated when taken with standard antidepressant treatment? Researchers will compare psychobiotic capsules with placebo capsules to see whether psychobiotics improve depression symptoms when used together with standard antidepressants. Participants will: 1. Continue taking their prescribed antidepressant medicine. Be randomly assigned to receive either a psychobiotic capsule or a placebo capsule once daily for 6 weeks. 2. Complete depression assessments at the start of the study and again at 3 and 6 weeks. 3. Attend regular follow-up visits so researchers can monitor symptoms, side effects, and overall progress

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: f
View:

• Patients diagnosed with major depressive disorder (According to Diagnostic \& Statistical Manual-5 criteria (as per operational definition)

• Age 18 to 60 years

• Both genders

• Patients who are able to speak and understand Urdu/ English language.

• Patients who are on stable doses of oral selective serotonin reuptake inhibitors for at least two weeks prior to enrollment in the study

• Patients with cut off score of \> 24 as assessed by 17 item clinician administered Hamilton depression rating scale.

Locations
Other Locations
Pakistan
Allama Iqbal Medical College, Jinnah Hospital Lahore
RECRUITING
Lahore
Contact Information
Primary
Senior Registrar, Psychiatry Department
aroojfatima47@yahoo.com
+923314567690
Time Frame
Start Date: 2026-01-31
Estimated Completion Date: 2027-01-31
Participants
Target number of participants: 86
Treatments
Active_comparator: Interventional Arm
People who are recieving Psychobiotics as an adjunct to the standard treatment.
Placebo_comparator: Placebo Comparator
people who will be given placebo capsules along with standard treatment
Related Therapeutic Areas
Sponsors
Collaborators: Jinnah Hospital, Allama Iqbal Medical College
Leads: Dr Sadia yasir

This content was sourced from clinicaltrials.gov