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Clinical Trial Summary

The purpose of this study is to o determine whether the modified LP procedure reduces the incidence of PLPH to 5% or lower, to determine whether the modified LP procedure reduces the frequency of epidural blood patch (EBP) usage to 10% or lower of the PLPH population and to identify factors that may contribute to or reduce incidence of PLPH


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06062446
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact Jay-Jiguang Zhu, MD,PhD
Phone (713) 486-8000
Email Jay.Jiguang.Zhu@uth.tmc.edu
Status Not yet recruiting
Phase N/A
Start date October 20, 2023
Completion date August 31, 2025

See also
  Status Clinical Trial Phase
Withdrawn NCT00373074 - Epidural Blood Patch on the Resolution of Postdural Puncture Headache (PDPH) Phase 2/Phase 3
Recruiting NCT01481922 - What Needle Diameter Should Physician Use When They Perform Lumbar Puncture ? A Randomized Controlled Trial Phase 4
Completed NCT01977898 - Incidence of Headache Following an Unintentional Dural Puncture N/A
Completed NCT03960749 - Headache After Diagnostic Lumbar Puncture N/A