EFFICACY OF ANSA (Experimental Drug) & CRAN MAX (Control Drug) SACHET
NCT05572268 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2022-10-07
Summary
I
This clinical trial aims to VIVO AND IN VITRO COMPARATIVE STUDY ON EFFICACY OF ANSA (experimental drug) \& CRAN MAX (control drug) SACHET IN UNCOMPLICATED UTI in females. The main question\[s\] it aims to answer are:
• Hypothesis I ANSA is an effective therapy for uncomplicated UTI treatment and inhibits or kills E.coli and other organisms in vitro and in vivo Null Hypothesis ANSA is not an effective therapy for uncomplicated UTI treatment and couldn't inhibit or kill E.coli and other organisms in vitro and in vivo Hypothesis II Cran Max is an effective therapy for uncomplicated UTIs and inhibits or kills E.coli and other organisms in vitro and in vivo Null Hypothesis Cran Max is not an effective therapy for uncomplicated UTI treatment and couldn't inhibit or kill E.coli and other organisms in vitro and in vivo
Conditions
- Treatment Compliance
Interventions
- DRUG
-
to evaluate the safety and efficacy of Ansa for the treatment of UTi and control of Ecoli infection
to evaluate the safety and efficacy of Cranmax for the treatment of UTi and control of Ecoli infection
Sponsors & Collaborators
-
Shifa Ul Mulk Memorial Hospital
lead OTHER
Principal Investigators
-
Misbah Ahmed, BEMS · Jinnah University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 15 Years
- Max Age
- 70 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-08-12
- Primary Completion
- 2024-08-12
- Completion
- 2024-08-12
Countries
- Pakistan
Study Locations
More Related Trials
-
to Assess the Eradication Rate of 14-day Bismuth/Amoxicillin/PCAB Triple Therapy for the Treatment of Helicobacter Pylori Infection
NCT07142798 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
A Study to Evaluate the Safety and Effectiveness of Levofloxacin Compared With Ciprofloxacin in Patients With Chronic Bacterial Prostatitis
NCT00236808 ·Status: COMPLETED ·Phase: PHASE3
-
Study Evaluating Safety and Tolerability of Allocetra-OTS in Patients With COVID-19
NCT04659304 ·Status: UNKNOWN ·Phase: PHASE1
-
PA Tolerability, Safety and Pharmacokinetics in Healthy Volunteers
NCT04174937 ·Status: COMPLETED ·Phase: PHASE1
-
Susceptibility-guided Bismuth Quadruple Therapy for Multiple-resistant Helicobacter Pylori Strains
NCT06687473 ·Status: COMPLETED ·Phase: PHASE4
-
A Trial of HRS-8427 in the Treatment of Adults With Complicated Urinary Tract Infection, Including Acute Pyelonephritis
NCT06569056 ·Status: RECRUITING ·Phase: PHASE3
-
Genotypic Resistance Guided Versus Susceptibility Testing Guided Therapy for the First-line Eradication of H. Pylori
NCT03556254 ·Status: UNKNOWN ·Phase: PHASE4
-
Study of Levofloxacin-based Concomitant Therapy for H. Pylori Eradication in Diabetic Patients
NCT02466919 ·Status: COMPLETED ·Phase: PHASE4
-
Susceptibility Testing Guided Versus Empirical Therapy for Refractory H. Pylori Infection
NCT04332848 ·Status: RECRUITING ·Phase: PHASE4
-
Antimicrobial Susceptibility Testing Guided Therapy Versus Empirical Therapy for the Rescue Treatment of Helicobacter Pylori Infection
NCT03565484 ·Status: UNKNOWN ·Phase: PHASE4
-
Moxifloxacin Versus Ofloxacin Plus Metronidazole in Uncomplicated Pelvic Inflammatory Disease: Multicenter Randomized Controlled Trials
NCT01799356 ·Status: COMPLETED ·Phase: PHASE4
-
Levofloxacin as an Empirical Therapy in Patients With Complicated Urinary Tract Infections
NCT03160807 ·Status: UNKNOWN ·Phase: PHASE4
-
Second Line Bismuth Containing Quadruple Therapy With Supplementary Probiotic
NCT05577572 ·Status: UNKNOWN ·Phase: NA
-
A Study Comparing Doxycycline and Levofloxacin for Treating COPD Exacerbations
NCT06915688 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Safety and Efficacy of Cefecin Tab. in Patients With Acute Sinusitis
NCT04664803 ·Status: TERMINATED ·Phase: PHASE4
-
Finafloxacin 300 mg Twice a Day (b.i.d.) Versus Ciprofloxacin 250 mg Twice a Day (b.i.d) in Patients With Lower Uncomplicated UTI (uUTI)
NCT00722735 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacies of Hybrid and High-dose Dual Therapies for the First-line Anti-H Pylori Treatment
NCT05152004 ·Status: COMPLETED ·Phase: NA
-
A Trial Comparing Moxifloxacin Versus Levofloxacin Plus Metronidazole In Uncomplicated Pelvic Inflammatory Disease
NCT00453349 ·Status: COMPLETED ·Phase: PHASE3
-
A Comparison of the Effectiveness and Safety of Levofloxacin to That of Ciprofloxacin in Treating Complicated Urinary Tract Infection and Acute Pyelonephritis.
NCT00210886 ·Status: COMPLETED ·Phase: PHASE3
-
A Multi-center, Randomized, Double-blind, Double-dummy Clinical Study to Evaluate the Safety and Efficacy of Prulifloxacin Film-coated Tablet for the Treatment of Acute Uncomplicated Lower Urinary Tract Infection With Levofloxacin Hydrochloride Tablet as Active Control
NCT02439632 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of 14-day Concomitant Therapy for Helicobacter Pylori Infection
NCT04991584 ·Status: UNKNOWN ·Phase: NA
-
A Study of the Safety and Effectiveness of Levofloxacin Compared With Lomefloxacin in the Treatment of Complicated Urinary Tract Infections
NCT00258102 ·Status: COMPLETED ·Phase: PHASE3
-
Comparing the Efficacy of Hybrid, High-dose Dual and Bismuth Quadruple Therapies
NCT03779074 ·Status: COMPLETED ·Phase: PHASE3
-
Urinary Bactericidal Activity of 4 Doses of Levofloxacin Against Fluoroquinolone-Resistant E. Coli
NCT00376376 ·Status: COMPLETED ·Phase: NA
-
Levofloxacin Plus Metronidazole Suppositories Versus Levofloxacin Co-administered with Metronidazole Tablets in Chronic Endometritis
NCT06650540 ·Status: NOT_YET_RECRUITING ·Phase: NA