Viewing Study NCT06644105


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Study NCT ID: NCT06644105
Status: COMPLETED
Last Update Posted: 2024-10-16
First Post: 2024-10-11
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Pharmacokinetic Study of Cefditoren Pivoxil in Breast Milk and Blood of Lactating Women
Sponsor: West China Second University Hospital
Organization:

Study Overview

Official Title: Pharmacokinetic Study of Cefditoren Pivoxil in Breast Milk and Blood of Lactating Women
Status: COMPLETED
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: RID
Brief Summary: The goal of this clinical trial is to provide a theoretical basis for the rational use of cefditoren pivoxil in lactating women by conducting a pharmacokinetic study of cefditoren in the blood and milk of these women. The main questions it aims to answer are:

Can lactating women use cefditoren pivoxil? Is cefditoren distributed in breast milk?

12 Participants will:

Take cefditoren pivoxil tablets 200mg after a meal, and collect breast milk and plasma over certain time periods.
Detailed Description: This study is a single-center, single-sequence, open-label pharmacokinetic study involving Chinese healthy lactating subjects. It aims to investigate the exposure of cefditoren in blood and milk in lactating women. The M/P (milk to plasma) ratio was estimated through the area under the plasma and milk concentration-time curves (AUC) \[6\], and the infant's exposure (Relative Infant Dose,RID) was estimated as the product of the actual milk production and the average milk drug concentration, normalized by body weight and expressed as a percentage of the mother's dose adjusted for body weight. By studying the pharmacokinetics of cefditoren in blood and milk, the study provides a theoretical basis for the rational use of cefditoren pivoxil in lactating women.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: