An Open Clinical Trial of the Safety and Efficacy of the Drug Fluorothiazinone, 300 Mg Tablets with the Participation of Adult Patients with Chronic Bacterial Cystitis"

NCT ID: NCT06815549

Last Updated: 2025-02-07

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 280 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-02-17
• Study Completion Date: 2025-12-31

Brief Summary

This study is designed to evaluate the safety, clinical efficacy and antibacterial activity of the drug Fluorothiazinone, 300 mg tablets, (Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation) in the mode of antibacterial monotherapy with the participation of adult patients with chronic bacterial cystitis.

The main objectives of this study are:

1. To evaluate the safety of the use of the drug Fluorothiazinone according to the indicators

1. adverse events/reactions;

2. serious adverse events/reactions;

3. deviations from clinical and laboratory parameters.

2. To evaluate the therapy effectiveness:

1. clinical cure - complete resolution or improvement of the signs and symptoms of chronic cystitis that were present at baseline and the absence of new symptoms requiring antimicrobial therapy on days 7, 14 and 28 after the start of therapy;

2. the timing of the disappearance of symptoms according to the patient's subjective feelings;

3. microbiological response when comparing pre-treatment and post-treatment cultures;

4. changes on VAS (visual analogue scale) for pain intensity determination;

5. changes on PUF (Pelvic pain and urgency/frequency patient symptom scale) for assessing symptoms by patients;

6. changes on ACSS (acute cystitis symptom scale);

7. development of relapses within 90 days after the start of therapy.

3. To collect clinical isolates of pathogens for molecular genetic analysis. The identification of DNA and the determination of the bacterial genotype will allow us to assess the microbiological outcomes such as relapse or reinfection.

4. To determine the sensitivity of the obtained isolates to antibiotics.

Conditions

P. Aeruginosa; Baumannii; Klebsiella Pneumonia; E.coli Infections; Enterococcus Faecalis Infection; Chronic Bacterial Cystitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Drug: Fluorothiazinone, tablets 300 mg

Treatment arm patients will receive Fluorothiazinone, tablets 300 mg at a dose 1200 mg/day (2 tablets twice a day) for 14 days.

Group Type: EXPERIMENTAL

Fluorothiazinone, tablets 300 mg

Intervention Type: DRUG

patients will receive Fluorothiazinone, tablets 300 mg at a dose 1200 mg/day (2 tablets twice a day) for 14 days

Comparator: Nitrofurantoin

Comparison arm patients will receive Nitrofurantoin in accordance with the instructions for medical use.

Group Type: ACTIVE_COMPARATOR

Nitrofurantoin 100 MG

Intervention Type: DRUG

Comparison arm patients will receive Nitrofurantoin in accordance with the instructions for medical use.

Interventions

Fluorothiazinone, tablets 300 mg

patients will receive Fluorothiazinone, tablets 300 mg at a dose 1200 mg/day (2 tablets twice a day) for 14 days

Intervention Type: DRUG

Nitrofurantoin 100 MG

Comparison arm patients will receive Nitrofurantoin in accordance with the instructions for medical use.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patient's written consent to participate in the study in accordance with the current legislation.

2. The ability to understand the requirements for the study participants, the willingness to follow the procedures according to the Study Protocol.

3. Female Patients, at least 18 years old.

4. Ambulatory treatment, absence of indications for emergency hospitalization during the period of inclusion in the study for the infection under study.

5. Bacterial cystitis, a history of chronic recurrent bladder infection.

6. The presence of symptoms characteristic of exacerbation of chronic cystitis: pain syndrome (pain in the lower abdomen, when urinating), dysuric symptoms (frequent urination, pain or burning when urinating, imperative urge to urinate, feeling of incomplete emptying of the bladder). 6 points or higher when assessing the characteristic symptoms on the ACSS scale.

7. Consent of patients with preserved reproductive potential to use effective methods of contraception using one of the following methods: abstinence, intrauterine device, oral/ injectable contraceptive, subcutaneous implant or double barrier method (condom with local contraceptive) for the period of participation in the study.

8. Negative pregnancy test result before randomization for female patients with preserved reproductive potential.

Exclusion Criteria

1. Inability to read in Russian; inability or unwillingness to understand the essence of the research. Any other conditions that limit the validity of obtaining informed consent or may affect the volunteer's ability to participate in the study.

2. Participation in any other study in the last 90 days;

3. Presence of an infection of another organ other than a bladder infection, such as endocarditis, osteomyelitis, abscess, meningitis, pneumonia, etc.

4. Symptoms requiring hospitalization (macrohematuria, concomitant diseases that complicate the course of the disease).

5. Cystocele of 3-4 degrees.

6. Treatment with Nitrofurantoin for 30 days before randomization.

7. Mental illness (registered by a psychiatrist according to medical records).

8. Treatment with hormonal drugs (with the exception of hormonal contraceptives, hormone replacement therapy, topical medications) for the last 10 days.

9. Autoimmune diseases or systemic connective tissue diseases in the anamnesis, requiring the appointment of immunosuppressive therapy.

10. Recipients of solid organs or tissues (bone marrow or peripheral blood stem cells).

11. Taking immunosuppressive drugs and/or immunomodulators for 6 months prior to the start of the study.

12. The presence of congenital or acquired immunodeficiency (AIDS, etc. according to medical history).

13. History of malignant neoplasms, with the exception of basal cell or squamous cell epithelial carcinomas of the skin, which were removed without signs of metastasis more than 3 years ago.

14. Blood donation (450 ml or more of blood or plasma) less than 2 months before the start of the study.

15. Planned hospitalization and / or surgical intervention during the period of participation in the study, as well as 4 weeks before the expected date of drug administration.

16. The presence of a concomitant disease that may affect the evaluation of the results of the study or which, in the opinion of the investigator, will not allow the patient to participate in the study or may affect the conduct of the study and / or its results (including the assessment of safety parameters), any conditions that, in the opinion of the medical investigator, may be a contraindication to participating in the study.

17. Pregnancy or breast-feeding.

18. Taking any long-acting systemic antibiotic (i.e., with a frequency of administration no more than once a day) for less than 12 hours before randomization.

19. The need at the time of randomization for additional systemic antimicrobial therapy (including antibacterial, antifungal therapy) other than treatment with the investigational drug, with the exception of a single oral administration of any antifungal drug for the treatment of vaginal candidiasis.

20. Lactose intolerance, lactase deficiency or glucose-galactose malabsorption, allergy to the components of the studied drug / reference drug in the anamnesis.

21. Contraindications to the use of Nitrofurantoin (severe renal excretory function disorders, renal insufficiency, oliguria, glucose-6-phosphate dehydrogenase deficiency, hypersensitivity to Nitrofurantoin, stage II-III heart failure, liver cirrhosis, chronic hepatitis, acute porphyria).

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

N.F. Gamaleya NRCEM, Health Ministry of the Russian Federation

Role: CONTACT

info@gamaleya.org

+7 (499) 193-30-01

Other Identifiers

07-FT-2024

Identifier Type: -

Identifier Source: org_study_id