Skip to main content
Clinical Trials/ITMCTR2000004035
ITMCTR2000004035
Not yet recruiting
Phase 1

A Randomized Controlled Clinical Study on Treatment of Acute Simple Urinary Tract Infection of Xiajiao Damp-Heat Type with Niaogan Fang

Shanghai Traditional Chinese Medicine Hospital0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Shanghai Traditional Chinese Medicine Hospital
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
Shanghai Traditional Chinese Medicine Hospital

Eligibility Criteria

Inclusion Criteria

  • (1\) Aged 18 to 50 years old;
  • (2\) Meet the Western diagnostic criteria for UTI under acute uncomplicated conditions, that is, the duration of the disease does not exceed 72 hours;
  • (3\) The result of bacterial culture is levofloxacin sensitive (bacterial culture and clinical treatment will be carried out at the same time);
  • (4\) TCM differentiation is Xiajiao damp\-heat syndrome;
  • (5\) Did not receive antibiotic treatment within 48 hours before being selected;
  • (6\) Not pregnant or breastfeeding;
  • (7\) Sign the written informed consent of the clinical trial.

Exclusion Criteria

  • (1\) Allergy to test drugs or quinolones;
  • (2\) Have a history of bacterial culture that is not sensitive to levofloxacin;
  • (3\) Diagnosed as complicated UTI disease;
  • (4\) Patients suffering from urinary calculi or obstruction, urinary tuberculosis, renal papillary necrosis, perinephric abscess or neurogenic bladder;
  • (5\) Accompanied by symptoms of vaginitis, genital ulcers or gonorrhea;
  • (6\) Combined with severe heart and lung disease, liver and kidney disease, advanced tumor and other serious or progressive diseases;
  • (7\) Suffer from neurological or mental illness, unable to cooperate;
  • (8\) Combined use of other antibacterial drugs;
  • (9\) Women who are pregnant, breastfeeding, or planning to become pregnant;
  • (10\) Participate in another clinical trial within three months before being selected.

Outcomes

Primary Outcomes

Not specified

Similar Trials