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Sugar water shot may ease sciatica pain in ER

NCT ID NCT07588126

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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study tested whether an ultrasound-guided injection of sugar water around the sciatic nerve could safely reduce sciatica pain in the emergency department. Researchers enrolled 69 adults with acute sciatica and followed up 72 hours later. The goal was to see if the procedure is feasible and safe, and whether it might lower pain in the short term.

What this could mean

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

Active substance
dextrose in water solution (sugar water)
What this could lead to
If this works, it could offer a simple, non-drug option for quickly reducing sciatica pain in the emergency room.
What could go wrong
This is a small, early feasibility study with only 69 participants and no control group. The results may not apply to everyone, and long-term benefits or risks are unknown.

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

69 people

The number who actually took part.

Started

Jan 2024

Finished

Feb 2025

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 years and older

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: * Age 18 years or older * Clinically diagnosed acute sciatica, defined as pain and/or paresthesias in a -sciatic nerve distribution * Willing to undergo the injection procedure * Verbal informed consent provided prior to enrollment * Adequate sonographic visualization of the sciatic nerve in the transgluteal window confirmed on screening ultrasound Exclusion Criteria: * Fever or signs of systemic infection * Suspected spinal infection * Suspected spinal malignancy * Signs or symptoms of cauda equina syndrome * Acute traumatic mechanism of pain * Localized infection or skin breakdown at the proposed injection site * Known allergy to study injectate (5% dextrose in water) or procedural materials * Refusal to participate * Inability to adequately visualize the target anatomy on ultrasound for safe injection

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Kaiser Permanente

    San Diego, California, 92123, United States

More trials for these conditions

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