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NCT07093151Enrolling by invitation

Comparison of Post-Craniotomy Blood Pressure Targets

COMparison of Postcraniotomy Blood pressurE Target Effectiveness (COMPETE)

Source: ClinicalTrials.gov · Last updated 21 Apr 2026

Brief summary (registry, in English)

The goal of this pragmatic clinical trial is to learn if a more intensive or more liberal blood pressure target after surgery is more effective in improving patient outcomes for adults undergoing craniotomy for removal of a brain tumor. There is little evidence to help doctors decide the best post-operative blood pressure target for their patients. The main question this study aims to answer is if patients with a post-operative systolic blood pressure target of \<160 mmHg will have a shorter hospital length of stay than those with a blood pressure target of \<140 mmHg, without increasing the rate of post-operative bleeding in the brain.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
500 (estimated)
First submitted
19 Jul 2025
Start date
15 Apr 2026
Primary completion date
30 Jun 2028
Lead sponsor
Vanderbilt University Medical Center
NCT number
NCT07093151

What you commit to

  • Study type: Interventional
  • Planned participants: 500
  • From 15 Apr 2026 to the primary completion date, 30 Jun 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Declines to consent
  • Attending decisions based on intraoperative findings (i.e. attending physician does not have equipoise that either blood pressure threshold would be acceptable for the post-operative care of the patient).
  • Patient is a prisoner
  • Patient is known to be pregnant

Who the study is looking for

  • Age ≥ 18 years old
  • Undergoes craniotomy for resection of an intradural brain tumor scheduled using any of the following Current Procedural Terminology (CPT) codes: 61304, 61305, 61330, 61333, 61510, 61512, 61516, 61518, 61519, 61520, 61521, 61524, 61526, 61530, 61545, 61580, 61581, 61582, 61583, 61584, 61585, 61586, 61590, 61591, 61592, 61595, 61596, 61597, 61598, 61600, 61601, 61605, 61606, 61607, 61608, 61615, 61616

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Vanderbilt University Medical Center
Coordinator of this site? Confirm its status
NashvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.