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Which anesthesia gets you home faster after ankle surgery?

NCT ID NCT07460310

Symptom relief Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang 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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study will compare three types of anesthesia for people having ankle surgery: total intravenous anesthesia with a nerve block, general anesthesia with a nerve block, and spinal anesthesia. The goal is to see which method allows patients to recover and leave the hospital the quickest. About 200 adults will take part across multiple hospitals.

What this could mean

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

Active substance
Anesthesia (total intravenous, balanced general, or spinal)
What this could lead to
If successful, this could identify the best anesthesia method for ankle surgery, helping patients recover faster and go home sooner.
What could go wrong
This is an early-stage trial not yet recruiting, so results are uncertain. The findings may not apply to all patients or surgeries.

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

About 200 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

Dec 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: * Full understanding of the study procedures and methods, with a signed written informed consent form. * Aged 18 to 65 years, of either sex. * Scheduled for elective unilateral minimally invasive ankle surgery. * American Society of Anesthesiologists (ASA) physical status classification I or II. * Body Mass Index (BMI) between 16 and 32 kg/m\^2 Exclusion Criteria: * Known hypersensitivity or allergy to any study medications or existing contraindications to anesthesia. * Chronic obstructive pulmonary disease (COPD) or unstable asthma. * History of difficult airway management, poorly controlled gastroesophageal reflux disease (GERD), or a known risk of aspiration. * Anticipated surgical duration exceeding 3 hours. * History of chronic preoperative opioid use or dependence. * History of severe postoperative adverse reactions (e.g., severe postoperative nausea and vomiting). * Pregnancy or lactation. * History of seizure disorders or epilepsy. * Severe peripheral neuropathy. * Any other condition that, in the opinion of the investigator, would preclude safe participation in the study.

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Conditions

The condition(s) this trial relates to.

agnosia ankle injury

As listed by the trial registrant

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

Ankle (ligaments); instability (old injury) Ankle arthroscopy Ankle sprain ERAS Pain management

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

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