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Correlation Studies on Human Body Composition Based on Bioequivalence or Pharmacokinetic Trials

Recruitingn/aAges 18 Years - 65 YearsAllSecond Affiliated Hospital of Wenzhou Medical Uni…
NCT07611929 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The aim of this observational study is to investigate the impact of body composition on the absorption, distribution, and metabolism of drugs. The primary question it seeks to answer is: Does body composition affect the absorption, distribution, and metabolism of drugs? By combining pharmacokinetic parameters and adverse drug reactions, the study will analyze differences in the metabolism of drugs under various body composition conditions. During the Phase I clinical trial, under the guidance of the researchers, subjects will use the non-invasive InBody S10 body composition analyzer to obtain body composition data, including but not limited to inorganic salts, muscle mass, lean body mass, body weight, and body fat percentage.

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Participants who have been successfully enrolled in the bioequivalence trials of Progesterone Sustained-release vaginal gel； 2. Have signed the informed consent form, have a full understanding of the content, process, and risks of this study, and can communicate well with the researchers. Exclusion Criteria:1: 1）Participants who may not be able to complete the study for other reasons or are deemed by the investigator to be unsuitable for participation in this study.
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What it tests

  • Not listed
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Where

1 site
The Second Affiliated Hospital and Yuying Children's Hospital Affiliated to Wenzhou Medical University
Wenzhou, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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