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Randomized Study of Two Dosage Forms (Oral Powder and Capsule) of "Chondroitin + Glucosamine Sulfate" Produced by the Laboratory EMS When Compared to the Product Condroflex (Oral Powder and Capsules) Produced by Laboratory Zodiac in the Treatment of Osteoarthrosis.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00860873
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:22.039769+00:00
Published At
2013-02-25T00:00:00+00:00
Record Updated At
2013-02-25
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Osteoarthrosis"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2013-02-25"
protocolSection.identificationModule.nctId
"NCT00860873"
protocolSection.identificationModule.officialTitle
"Randomized Study of Two Dosage Forms (Oral Powder and Capsule) of \"Chondroitin + Glucosamine Sulfate\" Produced by the Laboratory EMS When Compared to the Product Condroflex (Oral Powder and Capsules) Produced by Laboratory Zodiac in the Treatment of Osteoarthrosis."
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Osteoarthrosis (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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