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Brain surgery anesthesia showdown: which drug works best?

NCT ID NCT07105618

Symptom relief Sponsor: Zagazig University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Aug 25, 2026 · Updated 2 times

Summary

This study compares three different drugs (dexmedetomidine, fentanyl, and magnesium sulphate) used alongside propofol anesthesia for brain surgery. The goal is to see which combination reduces the amount of propofol needed and improves patient outcomes. 108 adults undergoing elective brain tumor removal will participate.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

120 people

The number who actually took part.

Started

Aug 2025

Expected to finish

Jun 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

21 to 60 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patient acceptance. * Physical status: American Society of Anesthesiologists Physical Status (ASA) 1\& II. * Body mass index ≤ 30 kg/m2. * Type of operation: elective craniotomy for brain tumor resection. * Duration of surgery: within 4 hours. Exclusion Criteria: * Patient with hemodynamic instability or anticipated postoperative mechanical ventilation. * Patients with a known history of allergy to the study drugs. * Advanced hepatic, renal, cardiovascular, and neurologic diseases. * Patients with chronic opioid use.

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Conditions

The condition(s) this trial relates to.

brain neoplasm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Anesthesia

Contacts and locations

Locations

  • Zagazig university hospital

    Zagazig, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.