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The Effect of Jincaopian Tablets on Chronic Pelvic Pain After Pelvic Inflammatory Disease

CompletedPhase 2NCT05460546
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This phase II trial attempts to evaluate the efficacy and safety of Jincaopian Tablets in the treatment of subjects with chronic pelvic pain after pelvic inflammatory disease.

Study details

Official title
A Multicenter, Randomized, Double-blind, Dose-parallel, Placebo-controlled Phase II Clinical Trial to Evaluate the Efficacy and Safety of Jincaopian Tablets in Subjects With Chronic Pelvic Pain After Pelvic Inflammatory Disease
Interventions
  • Drug: Jincaopian Tablets high dose
  • Drug: Jincaopian Tablets low dose
  • Other: Placebo
Sponsor
Beijing Konruns Pharmaceutical Co., Ltd.
Start date
2021-01-19
Primary completion
2021-11-30
Sex
Female
Age range
from 18 Years to 55 Years
Results posted
No results posted in this snapshot
Countries
China
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Meet the diagnostic criteria for chronic pelvic pain sequelae of pelvic inflammatory disease; * The average VAS score of pain in the week before enrollment is ≥4; * The McCormack scale of physical signs at the time of enrollment is 4 to 12 points (including 4 points and 12 points); * Women aged 18 to 55 (including 18 and 55) with a history of sexual life; * Voluntarily participate in this clinical trial, give informed consent and sign the informed consent form. Exclusion Criteria: * Pelvic inflammatory disease (acute attack); * Pregnant or lactating women, women of childbearing age who are unwilling to take effective measures to prevent pregnancy during the trial and within 3 months after the trial; * Critically ill or with surgical indications; * Previously diagnosed with cervical intraepithelial neoplasia, primary/secondary dysmenorrhea, pelvic stasis syndrome and chronic pelvic pain caused by other non-pelvic inflammatory diseases; * Complicated with specific vaginitis such as vulvovaginal candidiasis, trichomonas vaginitis, bacterial vaginosis, etc.; * Gynecological tumors (maximum diameter of uterine fibroids greater than 3cm and submucosal fibroids), endometriosis, adenomyosis, acute cervicitis, tuberculous pelvic inflammatory disease, interstitial cystitis and other diseases related symptoms; * Placement of intrauterine device in the past 3 months; absence of uterus and bilateral appendages; * Received related treatment or took drugs with similar functions and indications within 14 days before the introduction; * Have a history of allergy to the components of the test drug; * Participated in other clinical trials within the past 3 months; * The investigator believes that it is not suitable to participate in this clinical trial.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05460546