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NCT Number: NCT06632587

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 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).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Thomas Jefferson University Hospitals

Philadelphia, Pennsylvania, 19107, United States

Location status: Recruiting

Location contact

Pious Patel, MD

CONTACT

(215) 955-7000

About this study

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).

The primary endpoint involves a comprehensive evaluation of long-term functional outcomes at 6 months post-injury ("injury" defined as "acute traumatic injury or source of increased intracranial pressure secondary to stroke or intracranial hemorrhage"). This assessment aims to determine whether the timing of cranioplasty influences patients' neurological recovery, cognitive function, and overall quality of life. By comparing the outcomes of patients who undergo standard of care cranioplasty with those who undergo early cranioplasty, the study seeks to provide valuable insights into the potential benefits of the latter approach.

The findings of this research hold the potential to guide clinical practice and inform decision-making for patients who have undergone DHC. By considering a range of complications and incorporating a robust statistical framework, the study contributes to a more nuanced understanding of the advantages and disadvantages associated with different cranioplasty timing strategies.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults of age greater than or equal to 18 years at the time of acute traumatic injury or source of increased intracranial pressure secondary to stroke or intracranial hemorrhage necessitating decompressive hemicraniectomy (DHC)
  • Patient's cranial flap fulfills Craniectomy Contour Class A or B after 4 weeks postoperatively (doi:10.1227/ons.0000000000000689)
  • Medically optimized for general anesthesia/surgery

Exclusion criteria

  • Active systemic infection in weeks 6-8 post-DHC leading up to cranioplasty (e.g. pneumonia, urinary tract infection, soft tissue infection, bacteremia)
  • Cranial infection in the post-DHC period
  • Patient deemed not appropriate for early cranioplasty by attending neurosurgeon
  • Patient mortality prior to 8 weeks post-injury ("injury" defined as "acute traumatic injury or source of increased intracranial pressure causing brain injury secondary to stroke or intracranial hemorrhage")

Treatment and study plan

Early cranioplasty

Procedure

Cranioplasty is the surgical procedure to restore the skull after a decompressive hemicraniectomy. The latter procedure is employed as a life-saving measure to relieve intracranial pressure in patients with acute cranial injuries. Early cranioplasty is defined as being performed within 8 weeks following the decompressive hemicraniectomy.

Standard-of-care cranioplasty

Procedure

Cranioplasty is the surgical procedure to restore the skull after a decompressive hemicraniectomy. The latter procedure is employed as a life-saving measure to relieve intracranial pressure in patients with acute cranial injuries. Standard-of-care cranioplasty is defined as being performed after 3 months following the decompressive hemicraniectomy.

Primary outcomes

  1. Functional outcome at 6 months post-decompressive hemicraniectomy

    Time frame: 6 months post-decompressive hemicraniectomy

    modified Rankin scale outcome at 6 months post-decompressive hemicraniectomy

  2. Functional outcome at 12 months post-decompressive hemicraniectomy

    Time frame: 12 months post-decompressive hemicraniectomy

    modified Rankin scale outcome at 12 months post-decompressive hemicraniectomy

Secondary outcomes

  1. Post-cranioplasty seizure

    Time frame: 1 month post-cranioplasty

    Post-cranioplasty seizure occurrence, diagnosed clinically or on EEG

  2. Post-cranioplasty hydrocephalus

    Time frame: 1 month post-cranioplasty

    Post-cranioplasty hydrocephalus or need for cerebrospinal fluid diversion

  3. Post-cranioplasty return to operating room

    Time frame: 1 month post-cranioplasty

    All-cause return to operating room after cranioplasty

  4. Post-cranioplasty infection

    Time frame: 12 months post-cranioplasty

    Surgical site or intracranial infection after cranioplasty

  5. Post-cranioplasty disposition

    Time frame: 12 months post-cranioplasty

    Post-cranioplasty disposition (home, acute rehab, subacute rehab, death)

  6. Post-cranioplasty length of hospital stay

    Time frame: 12 months post-cranioplasty

    Post-cranioplasty length of hospital stay

  7. Readmission within 30 days post-cranioplasty

    Time frame: 30 days post-cranioplasty

    Readmission within 30 days post-cranioplasty

Study contacts

Contact information is provided by the study sponsor or research team.

Pious Patel, MD

CONTACT

[email protected]

(215) 955-7000

Sponsors and collaborators

Lead sponsor

Thomas Jefferson University

Other

Registry information

Official study title

Comparing Outcomes Between Early and Standard-of-care Delayed Cranioplasty After Decompressive Hemicraniectomy

Acronym: TIMELY

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Oct 9, 2024
Registry last updated
Jul 23, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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