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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: Recruiting NA study of Post-Lumbar Puncture Headache, sponsored by The University of Texas Health Science Center, Houston.
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, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
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
Primary Outcome
Participants will answer "Yes" or "No" in response to 1-2 questions: 1) Do you have a headache? 2) If you answered "Yes" to the previous question, does the headache get better when you sit up?
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 |
What NCT06062446 shows while recruiting
NCT06062446 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06062446's enrollment target sits among peer trials
100 841st of 2000 higher than 1,081 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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