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NCT05645302

Intensive Monitoring Scheme of Lidocaine Cataplasms

Status unknown Last updated 9 December 2022
What this trial tests

trial testing Lidocaine Cataplasms in Adverse Reaction to Drug in 200 participants. Status unknown.

Timeline
6 April 2022
Primary endpoint
31 October 2022
31 December 2022

Quick facts

Lead sponsorQianfoshan Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment200
Start date6 April 2022
Primary completion31 October 2022
Estimated completion31 December 2022
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Qianfoshan Hospital

Who can join

Eligibility, any sex, with Adverse Reaction to Drug. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this center, retrospective research methods are used to collect data. Patients who had used Lidocaine Cataplasms at least once were included consecutively. Taking the time when the patient first used Lidocaine Cataplasms as the starting time (the study baseline), collect the demographic characteristics of the patient, the medication scheme of Lidocaine Cataplasms and other information, as well as the medication safety and other information from the first medication to the end of medication or discharge (whichever occurs first).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Qianfoshan Hospital trials

Trials by the same sponsor.

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Data sources for this page

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