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Clinical Trial Summary

The goal of this clinical trial is to compare the effects of CMPAT and MAT in patients undergoing LP. Participants will be randomly assigned to either the CMPAT treatment group (group A) or the MAT treatment group (group B). Researchers will compare CMPAT treatment group and the MAT treatment group to see if the number of needle insertion attempts required for a successful LP, the puncture success rate, pain assessment in the back, head, and legs, and the occurrence of complications have different.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06418841
Study type Interventional
Source Fujian Medical University Union Hospital
Contact Yuan-Dong Zhuang
Phone 15260866029
Email zyd2013@qq.com
Status Not yet recruiting
Phase N/A
Start date October 28, 2024
Completion date October 28, 2025

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