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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: Recruiting NA study of Stroke and Craniocerebral Trauma, sponsored by Thomas Jefferson University.

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. According to ClinicalTrials.gov, the official US trial registry.

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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).

Primary Outcome

modified Rankin scale outcome at 6 months post-decompressive hemicraniectomy

Interventions

  • PROCEDURE Early cranioplasty
  • PROCEDURE Standard-of-care cranioplasty

Study Locations (1)

Pennsylvania

  • Thomas Jefferson University Hospitals - Philadelphia

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2024-09-01
Est. Completion 2027-09-01
Phase NA
Thomas Jefferson University

292 total trials

What NCT06632587 shows while recruiting

NCT06632587 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower).

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 a single indexed study location in 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.

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.

Where NCT06632587's enrollment target sits among peer trials

44 255th of 454 higher than 196 of 454 other Stroke trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Stroke 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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Source: ClinicalTrials.gov NCT06632587, the US trial registry maintained by the National Library of Medicine. NCT06632587 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.