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Studying the role of probiotic in the treatment of urinary tract infections in women

Studying the role of probiotic in the treatment of recurrent uncomplicated urinary tract infections in women

Status
Unknown
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025175
Enrollment
90
Registered
2020-05-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N390- Urinary tract infection, site notspecified

Interventions

Intervention1: Lactobacillus acidophilus (2 billion), Lactobacillus bulgaricus (1 billion), Bifidobactaterium bifidum (1 billion), and Fructooligosaccharides (100 mg): Each capsule contains: Lactobaci

Sponsors

Bangladesh Medical Research Council
Lead Sponsor
Purnava Ltd
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: i. Sex: female ii.Female suffering from only recurrent uncomplicated UTI iii. Patients have not received any antimicrobial and/or probiotic therapy within one month prior to enrollment in the study. iv. Non-pregnant women

Exclusion criteria

Exclusion criteria: i. Sex: Male ii. Status: Pregnant women ii. Patients received any antimicrobial and/or probiotic therapy within one month prior to enrollment in the study. iii. Patients having relevant interactions of prescribed antimicrobial agent or probiotics with concurrent medication or contraindications.

Design outcomes

Primary

MeasureTime frame
1. The number of patients is cured of UTI due to administration of probiotics/antibiotics. It will be based on absence or decreased severity of clinical signs-symptoms after completion of course of probiotics and antibiotics. 2.Identification of the organisms responsible for UTI and evaluation of the development of antibiotic resistance by expressing in percentage of antibiotic resistant E. Coli isolate from urine of symptomatic women.Timepoint: At Baseline, 2 weeks and 4 weeks

Secondary

MeasureTime frame
1. The micro biologically confirmed recovery of patients suffering from UTI. 2. Proportion of patientsâ?? experienced adverse events.Timepoint: At baseline, 2 weeks and 4 weeks

Countries

Bangladesh

Contacts

Public ContactAbu Syed Md Mosaddek

Uttara Adhunik Medical College

Drmosaddek1968@gmail.com1711483814

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026