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NCT06062446 · ClinicalTrials.gov registry record · NA
A Prospective Study of a Modified Lumbar Puncture (LP) Procedure That Reduces Post-Lumbar Puncture Headaches (PLPH) in Patients
A NA study of Post-Lumbar Puncture Headache, sponsored by The University of Texas Health Science Center, Houston.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT06062446 is a NA study of Post-Lumbar Puncture Headache that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 100 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06062446, a NA study of Post-Lumbar Puncture Headache, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study 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
Conditions Studied
Interventions
- PROCEDURE Modified Lumbar Puncture
Study Locations (1)
Texas
- The University of Texas Health Science Center at Houston - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2023-11-08 |
| Est. Completion | 2026-04-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06062446
The ClinicalTrials.gov registry entry for NCT06062446 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Post-Lumbar Puncture Headache appearing as the primary indexed condition, and to 1 intervention - of which Modified Lumbar Puncture is the first listed.
NCT06062446 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT06062446 about?
NCT06062446 is a clinical study titled "A Prospective Study of a Modified Lumbar Puncture (LP) Procedure That Reduces Post-Lumbar Puncture Headaches (PLPH) in Patients". 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...
What is the current status of trial NCT06062446?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2023-11-08. Estimated completion is 2026-04-01.
What conditions does trial NCT06062446 study?
This clinical trial studies the following conditions: Post-Lumbar Puncture Headache.
What interventions are being tested in trial NCT06062446?
The interventions under investigation include: Modified Lumbar Puncture (PROCEDURE).
Who is sponsoring clinical trial NCT06062446?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06062446 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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