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This study is a multi-center, randomized, double-blinded, controlled trial with two parallel arms. The study aims to evaluate the efficacy and safety of Involucrata Liquid Tonic in patients with Postpartum Rheumatism.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Saussurea Involucrata Liquid Tonic | Experimental | Saussurea Involucrata Liquid Tonic 20ml/time, 2 times a day, orally on an empty stomach. Total treatments 8 weeks, followed up to 12 weeks. |
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| placebo of Saussurea Involucrata Liquid Tonic | Placebo Comparator | placebo of Saussurea Involucrata Liquid Tonic 20ml/time, 2 times a day, orally on an empty stomach. Total treatments 8 weeks, followed up to 12 weeks. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Saussurea Involucrata Liquid Tonic | Drug | This product is a single preparation of Saussurea Involucrata Liquid Tonic. It is used for rheumatoid arthritis, rheumatoid arthritis and dysmenorrhea caused by insufficient kidney yang and cold-damp stasis. |
| Measure | Description | Time Frame |
|---|---|---|
| VAS (visual analog scale) | The number of cases with pain VAS (visual analog scale) improvement ≥30%/number of enrolled cases × 100%. | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| SF-36 | the MOS item short from health survey, SF-36 | 8 weeks |
| HADS | Hospital Anxiety and Depression Scale | 8 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| HAQ | Stanford Health Assessment Questionnaire | 8 weeks |
| VAS | Visual Analogue Score | 8 weeks |