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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01745328
Other study ID # WJUTI
Secondary ID
Status Recruiting
Phase N/A
First received December 5, 2012
Last updated December 7, 2012
Start date January 2009
Est. completion date July 2013

Study information

Verified date December 2012
Source Beijing Institute of Disease Control and Prevention
Contact Shiwei Liu, Dr
Phone 86-10-84739029
Email liushiwei1977@yeah.net
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Traditional Chinese Medicine (TCM) could be used to treat Recurrent urinary tract infection (RUTI).


Description:

Antibiotics and TCM are used to treat RUTI to evaluate treatment efficiencies.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date July 2013
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- uncomplicated RUTI

Exclusion Criteria:

- complicated RUTI

- other disease with urinary tract

- infection by pathogens other than bacteria

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
LVX-AMX
Subjects were treated with Levofloxacin, 200mg bid, Amoxicillin, 500mg tid for 1 week, followed by 3 week of placebo.
TCM
Subject is treated with TCM for 4 weeks.
LVX-AMX
treatment with placebo from 2 to 4 weeks.

Locations

Country Name City State
China Wangjing Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Institute of Disease Control and Prevention

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recovery of recurrent urinary tract infection Patients are checked at 4 weeks at the end of the treatment to confirm recovery of RUTI. 4 weeks after study drug start No
Secondary Urinary albumin Urinary albumin is checked in patient urine. 4 weeks after drug start No
Secondary WBC conversion Check the WBC count in patient urine. 4 weeks after drug start No
Secondary Urination frequency Checked for urination frequency at 4 weeks after drug start. 4 weeks after drug start No
Secondary Recurrence Patients are checked for recurrence rate at 6 months after drug start by telephone interview. 6 months after drug start No
Secondary urgency Check urgency 4 weeks after drug start 4 weeks after drug start No
See also
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Active, not recruiting NCT05537519 - Phage Therapy for the Treatment of Urinary Tract Infection Phase 1/Phase 2
Recruiting NCT06035601 - EHR-integrated rUTI Texting Platform N/A
Not yet recruiting NCT04285320 - Antibiotic Bladder Instillations vs. Oral Suppression for the Treatment of Recurrent Urinary Tract Infections Phase 4
Recruiting NCT03142295 - Controlled Human Urine Transfusion for UTI N/A
Recruiting NCT05895578 - Effect of a Probiotic on the Urinary Tract Microbiota of Participants With Recurrent Urinary Tract Infection. N/A
Completed NCT00214045 - Rigid Versus Flexible Cystoscopy in Women N/A
Enrolling by invitation NCT05551949 - Preventing Recurrent UTI With Vaginal Estrogen Phase 4