Viewing Study NCT06642129



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06642129
Status: RECRUITING
Last Update Posted: None
First Post: 2024-09-15

Brief Title: A Prospective Observational Study of Perioperative Lumbar Puncture Pressure and Shunt Valve Pressure Management in Patients with Communicating Hydrocephalus Undergoing Lumboperitoneal Shunt Surgery
Sponsor: None
Organization: None

Study Overview

Official Title: A Prospective Observational Study of Perioperative Lumbar Puncture Pressure and Shunt Valve Pressure Management in Patients with Traffic Hydrocephalus Undergoing Lumbopeitoneal Shunt Surgery
Status: RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: LPP-LPS
Brief Summary: Target population patients 18 years of age or older who require surgical treatment with lumboperitoneal shunt surgery for traffic hydrocephalus Estimated sample size 30 cases Study design this study is a multicenter prospective observational study with lumbar puncture pressure measurement before and during surgery and shunt valve setting pressure set according to the requirements of clinical practice in the hospital where it is performed and the collection of relevant data including preoperative lumbar puncture pressure intraoperative lumbar puncture pressure after anesthesia shunt valve initial pressure shunt valve pressure at 6 months pressure length of the intravertebral shunt and length of the intraperitoneal shunt Complications shunt effects and the number of shunt valve adjustments during the 6-month period were also observed and recorded
Detailed Description: None

Study Oversight

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