Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06632587 · ClinicalTrials.gov registry record · NA
Timing Impact of Early vs. Late Cranioplasty on Hemicraniectomy Outcomes
A NA study of Stroke and Craniocerebral Trauma, sponsored by Thomas Jefferson University.
- Recruiting
- Registry status
- NA
- Development phase
- 44
- Enrollment target
- 1
- Study location
NCT06632587 is a NA study of Stroke and Craniocerebral Trauma that is actively recruiting participants, run by Thomas Jefferson University. The registered enrollment target is 44 participants, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06632587, a NA study of Stroke and Craniocerebral Trauma, is actively recruiting participants, sponsored by Thomas Jefferson University.
- RECRUITING
- Registry status
- NA
- Development phase
- 44 participants
- Enrollment target
- 1
- Study location
Study Summary
This prospective, randomized study aims to comprehensively evaluate the impact of cranioplasty timing on postoperative complications and long-term functional outcomes following decompressive hemicraniectomy (DHC). The primary endpoint focuses on comparing the rates of various postoperative complications, including infection, seizures, return to the operating room, and the need for ventriculoperitoneal shunting, between patients undergoing standard of care cranioplasty (\>3 months after DHC) and those receiving early cranioplasty (within 8 weeks).
Conditions Studied
Interventions
- PROCEDURE Early cranioplasty
- PROCEDURE Standard-of-care cranioplasty
Study Locations (1)
Pennsylvania
- Thomas Jefferson University Hospitals - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2024-09-01 |
| Est. Completion | 2027-09-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06632587
The ClinicalTrials.gov registry entry for NCT06632587 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower). The listed sponsor is Thomas Jefferson University, which has 292 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Stroke appearing as the primary indexed condition, and to 2 interventions - of which Early cranioplasty is the first listed.
NCT06632587 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT06632587 about?
NCT06632587 is a clinical study titled "Timing Impact of Early vs. Late Cranioplasty on Hemicraniectomy Outcomes". This prospective, randomized study aims to comprehensively evaluate the impact of cranioplasty timing on postoperative complications and long-term functional outcomes following decompressive hemicraniectomy (DHC). The primary endpoint focuses on comparing the rates of various postoperative complicat...
What is the current status of trial NCT06632587?
This trial is currently recruiting. It is a NA study. The enrollment target is 44 participants. The study started on 2024-09-01. Estimated completion is 2027-09-01.
What conditions does trial NCT06632587 study?
This clinical trial studies the following conditions: Stroke, Craniocerebral Trauma, Intracranial Hemorrhages.
What interventions are being tested in trial NCT06632587?
The interventions under investigation include: Early cranioplasty (PROCEDURE), Standard-of-care cranioplasty (PROCEDURE).
Who is sponsoring clinical trial NCT06632587?
This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06632587 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Stroke
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Tracking a Tactile Signal Along the Nervous System
RECRUITING · NA
-
Transcranial Direct Current Stimulation (tDCS) With Verb Network Strengthening Treatment (VNeST) in Chronic Aphasia
RECRUITING · NA
-
Strategy Training for Individuals With Unilateral Neglect
RECRUITING · NA
-
Weight Loss and ExeRcise
RECRUITING · NA
-
Safety and Feasibility of an ExoNET for Supination Assistance for Stroke Survivors
RECRUITING · NA
-
Deep Brain Stimulation Motor Ventral Thalamus (VOP/VIM) for Restoration of Speech and Upper-limb Function in People With Subcortical Stroke
RECRUITING · NA
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.