Project description:Intervention 1: Patients in main group received standardized capsules containing in Apium graveolens L.fruit for 12 courses daily with 8h spans. They were informed of consumption instructions and time. Patients were closely observed in each of the twelve courses. Intervention 2: Patients in main group received standardized capsules containing in cellulose for 12 courses daily with 8h spans. They were informed of consumption instructions and time.;Treatment - Drugs;Placebo;Patients in main group received standardized capsules containing in Apium graveolens L.fruit for 12 courses daily with 8h spans. They were informed of consumption instructions and time. Patients were closely observed in each of the twelve courses.;Patients in main group received standardized capsules containing in cellulose for 12 courses daily with 8h spans. They were informed of consumption instructions and time. Primary outcome(s): The pain. Timepoint: Beforetreatment, 5 to 6 months after treatment. Method of measurement: Questionnaire. Study Design: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.

| 2492732 | ecrin-mdr-crc

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