RecruitingPhase 3NCT05970783
A Study of Jincaopian Tablets on Chronic Pelvic Pain After Pelvic Inflammatory Disease
A Multicenter, Randomized, Double-blind, Dose-parallel, Placebo-controlled Phase III Clinical Trial to Evaluate the Efficacy and Safety of Jincaopian Tablets in Subjects with Chronic Pelvic Pain After Pelvic Inflammatory Disease
Sponsor
Beijing Konruns Pharmaceutical Co., Ltd.
Enrollment
414 participants
Start Date
Nov 8, 2022
Study Type
INTERVENTIONAL
Conditions
Summary
The objective of this phase III trial to evaluate the efficacy and safety of Jincaopian Tablets in the treatment of subjects with chronic pelvic pain after pelvic inflammatory disease
Eligibility
Sex: FEMALEMin Age: 18 YearsMax Age: 50 Years
Inclusion Criteria5
- 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 50 (including 18 and 50) with a history of sexual life;
- Voluntarily participate in this clinical trial, give informed consent and sign the informed consent form.
Exclusion Criteria15
- 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 6 months after the trial;
- 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;
- 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;
- Liver function: ALT or AST>1.5 times the upper limit of normal value;Renal function:Scr>1.0 times the upper limit of normal value;
- Serum CA125 and erythrocyte sedimentation > 1.1 times the upper limit of normal value.
- Combined with serious cardiovascular, cerebrovascular, hematopoietic system and other serious diseases;
- Have an allergic history to the experimental drug;
- Have a long history of alcoholism or drug abuse;
- Intellectual disabilities or mental disorders;
- Participated in other clinical trials within the past 3 months;
- The investigator believes that it is not suitable to participate in this clinical trial.
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Interventions
DRUGJincaopian Tablets
Jincaopian Tablets 0.2g tid p.o.
OTHERPlacebo
Placebo 0.2g tid p.o.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05970783
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