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Clinical Observation of Relinqing Granule Combined with Ciprofloxacin in Treating Chronic Prostatitis

Clinical Observation of Relinqing Granule Combined with Ciprofloxacin in Treating Chronic Prostatitis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035212
Enrollment
Unknown
Registered
2020-08-03
Start date
2020-08-08
Completion date
Unknown
Last updated
2020-08-10

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

Conditions

Chronic prostatitis

Interventions

Sponsors

The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) The diagnostic criteria of type II and Type IIIA chronic prostatitis were met; (2) It is in accordance with the diagnostic criteria of dampness heat stasis and kidney deficiency syndrome; (3) The age ranged from 18 to 50 years old; (4) Patients with a course of disease >= 3 months and who had been treated before treatment could be included in the study only after stopping using all relevant Chinese and Western medicines for chronic prostatitis for at least 2 weeks; (5) Those who voluntarily participate in this clinical trial, and have informed consent and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with benign prostatic hyperplasia, prostate tumor, neurogenic bladder dysfunction, urethral malformation or stenosis, severe neurosis; (2) Patients with urinary tract infection and urethritis; (3) Other diseases such as ureter, bladder stones, inguinal hernia, pubitis, varicocele, epididymitis, rectocolonitis, lumbosacral myofascitis, etc. should be excluded if local pain is the main manifestation; (4) Patients with severe primary diseases such as cardiovascular, cerebrovascular, liver, kidney and hematopoietic system; (5) Psychiatric patients, diabetic patients, urinary calculi patients; (6) The subjects are participating in clinical trials of other drugs at the same time or using drugs with similar therapeutic effects as the trial drugs; (7) Allergic constitution (including drug allergy, food allergy and other allergic constitution); (8) The subjects were not willing to participate in the trial or could not cooperate with the treatment due to alcoholism and / or psychoactive substances, drug abusers and addicts, and avoiding spicy diet; (9) Those considered unsuitable for clinical trials by the researchers.

Design outcomes

Primary

MeasureTime frame
Concentration of ciprofloxacin and relinquin markers;NIH-CPSI;

Secondary

MeasureTime frame
Bacterial culture of prostatic fluid;

Countries

China

Contacts

Public ContactHuang Yu-Hong

The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine

hyh101@126.com+86 022-60637918

Outcome results

None listed

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