The purpose of this study is to evaluate the efficacy, safety of Qianjin Capsule of Gynaecology combined with antibiotics for pelvic inflammatory diseases (Damp-heat Stasis and Qi Deficiency Syndrome) for the short-term and long-term efficacy of traditional Chinese medicine in reducing the use of antibiotics, reducing the risk of clinical use of drugs.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
184
To evaluate the short-term and long-term efficacy of traditional Chinese medicine of Qianjin Capsule of Gynaecology in reducing the use of antibiotics, reducing the risk of clinical use of drugs.
The MCCormack scale scores of 184 subjects will be assessed
assessment of the 70% reduction rate after treatment
Time frame: Change from base line on the 56 days after discontinuation
The neutrophils of 184 participants will be assessed
assessment of neutrophils returning to normal reference range
Time frame: Change from base line on the 28 days of medication and 56 days after discontinuation
The whole blood reduced viscosity from hemorheological tests of 184 participants will be assessed
assessment of whole blood viscosity returning to normal reference range
Time frame: Change from base line on the 28 day of medication.
The plasma viscosity from hemorheological tests of 184 participants will be assessed
assessment of the plasma viscosity returning to normal reference range
Time frame: Change from base line on the 28 day of medication.
The fibrinogen determination from hemorheological tests of 184 participants will be assessed
assessment of the fibrinogen determination returning to normal reference range
Time frame: Change from base line on the 28 day of medication.
The CRP of 184 participants will be assessed
assessment of the CRP returning to normal reference range
Time frame: Change from base line on the 28 day of medication.
The volume of liquid on B-mode of 184 subjects will be assessed
The changes of the volume of liquid on B-mode at different observation points before and after treatment will be assessed
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Time frame: After 28 days of medication
The white blood cells of 184 participants will be assessed
assessment of the white blood returning to normal reference range
Time frame: Change from base line on the 28 days of medication and 56 days after discontinuation
The TCM syndrome scores of 184 subjects will be assessed
assessment of the 70% reduction rate after treatment
Time frame: Change from base line on the 56 days after discontinuation
The VAS score of 184 subjects will be assessed
assessment of the 70% reduction rate after treatment
Time frame: Change from base line on the 56 days after discontinuation