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Which anesthesia drug wakes you up faster after spine surgery?

NCT ID NCT07443163

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study compares two drugs, magnesium sulfate and dexmedetomidine, used alongside total intravenous anesthesia during spine surgery. The goal is to see which drug helps patients wake up and have their breathing tube removed faster. Forty adults scheduled for elective spine surgery will be randomly assigned to receive one of the two drugs. The results could help improve recovery after spine surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
magnesium sulfate and dexmedetomidine
What this could lead to
If this trial succeeds, it could help doctors choose the best anesthesia drug for faster recovery after spine surgery.
What could go wrong
This is a small early-stage trial with only 40 participants, so results may not apply to everyone. The drugs may also cause side effects like low blood pressure or slow heart rate.

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

Phase 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

About 40 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Ages

18 to 65 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: * American Society of Anesthesiologists (ASA) physical status I, II. * Scheduled for elective spine surgery up to two levels under general anesthesia Exclusion Criteria: * History of preoperative neuromuscular disease, hepatic impairment \[defined as a known diagnosis of liver cirrhosis, hepatitis with elevated liver enzymes (\>2 times upper standard limit), or Child-Pugh score B or C\], renal impairment \[defined as chronic kidney disease with an estimated glomerular filtration rate (eGFR) \<60 mL/min/1.73 m² or history of dialysis\], endocrinal disorders \[including uncontrolled diabetes mellitus (HbA1c \>8.5%), thyroid dysfunction (untreated hypo/hyperthyroidism), or adrenal insufficiency\], hematological disorder \[such as anemia (Hb \<10 g/dL), coagulopathies (INR \>1.5, platelet count \<100,000/mm³), or bleeding diathesis\] or cardiovascular dysfunction \[defined as history of ischemic heart disease, arrhythmias requiring treatment, heart failure (NYHA class II or higher), or uncontrolled hypertension (SBP \>160 mmHg or DBP \>100 mmHg)\]. * Any degree of heart block. * Known allergy to the study drugs. * Scoliosis surgery. * Cervical spine surgeries. * Surgeries with an anticipated duration of more than 4 hours. * Receiving magnesium supplementation. * Any Preoperative Disturbed consciousness level or cognitive dysfunction. * Drugs known to have a significant interaction with NMDAs. * Chronic use of opioids and current treatment with a β-blocker or calcium channel blocker.

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As listed by the trial registrant

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How to take part

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  1. The official record

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