Paracetamol and codiene

Added: Shemica Dipasquale - Date: 06.10.2021 20:07 - Views: 43127 - Clicks: 8251

Study record managers: refer to the Data Element Definitions if submitting registration or information. Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Contraception and fertility females only : females of child-bearing potential must be using at least one of the following reliable methods of contraception:. Hide glossary Glossary Study record managers: refer to the Data Element Definitions if submitting registration or information. Search for terms x. Save this study. Warning You have reached the maximum of saved studies Listing a study does not mean it has been evaluated by the U. Federal Government. Read our disclaimer for details. Last Update Posted : September 16, Study Description.

FDA Resources. Arms and Interventions. A single dose of active comparator will be administered to healthy male and female volunteers under fasting conditions before treatment arm 2 or after treatment arm 1 a wash-out interval of at least 7 days between the experimental drug administration. Outcome Measures. Secondary Outcome Measures : Area under the concentration vs. Eligibility Criteria. Female participants of non-child-bearing potential or in post-menopausal status for at least 1 year will be admitted.

For all female subjects, pregnancy test result must be negative at screening. Hormonal contraceptives for females will be allowed Investigative drug studies: participation in the evaluation of any investigational product for 3 months before this study. Contacts and Locations. Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials. More Information. A ClinicalTrials. National Library of Medicine U. National Institutes of Health U. Department of Health and Human Services. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Phase 1. Study Type :. Interventional Clinical Trial.

Actual Enrollment :. Study Start Date :. Actual Primary Completion Date :. Actual Study Completion Date :. September 16, Key Record Dates.

Paracetamol and codiene

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No effect of preoperative paracetamol and codeine suppositories for pain after termination of pregnancies in general anaesthesia