Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Arnica tested for wisdom tooth recovery: natural relief or sugar pill?

NCT ID NCT03944629

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether a homeopathic remedy called Arnica montana (SinEcch™) can reduce swelling and pain after having wisdom teeth removed. Fifty-three adults took either Arnica or a placebo (sugar pill) before and after surgery. Researchers measured facial swelling and pain levels over several days to see if the herb made a difference.

What this could mean

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

Active substance
Arnica montana (homeopathic remedy)
What this could lead to
If it works, this could offer a natural option to reduce swelling and pain after dental surgery.
What could go wrong
This is a small, completed trial with only 53 participants. Homeopathic remedies are highly diluted and often show no effect beyond placebo.

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.

Participants

53 people

The number who actually took part.

Started

Jan 2018

Finished

Jun 2022

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 40 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Subjects of either sex and of any race from the ages of 18 to 40 years. * Subjects for whom a decision has been made to extract 4 third molars, and who have at least 2 of third molar teeth classified as full or partially bony impacted in the mandible, and they will be evaluated to have at least 2 of third molar teeth classified as erupted or impacted (full or partially bony) in the maxilla under local anesthesia alone, local anesthesia and sedation, or local anesthesia and general anesthesia, all in an outpatient setting. 1. Full/complete bony: The entire tooth is below the level of the alveolar bone. The tooth is completely encased in bone so that when the gingiva is cut and reflected back, the tooth is not seen. Bone removal (large amounts) together with root sectioning will be needed to remove the tooth. 2. Partial bony: A portion of the height of the contour of the tooth is below the level of the alveolar bone. The superficial portion of the tooth is covered only by soft tissue, but the height of the tooth's contour is below the level of the surrounding alveolar bone. * Subjects must be physically able to tolerate conventional surgical procedures (ASA I/II). * Subjects must agree to follow the study protocol as shown by signing the informed consent form. Exclusion Criteria: * Subjects who are known to be pregnant or think they may be pregnant. (A urine pregnancy test will be performed on female subjects at Day 0 - Visit 1. Subjects testing positive will be excluded from study participation.) * Subjects with skeletal immaturity as determined by the medical history. * Subjects with self-reported current or history of substance abuse. * Subjects who are currently receiving any anti-inflammatory or pain medication chronically, or they suffer from a chronic pain condition. * Subjects with an allergy to Vicodin (or its constituents, acetaminophen and hydrocodone). * Subjects who are diagnosed with fibromyalgia. * Allergy to ragweed and other related plants. * Subjects with an allergy to hypromellose. * Non-English speaking patients

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for ARNICA are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

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

Contacts and locations

Locations

  • Tufts University School of Dental Medicine Department of Oral and Maxillofacial Surgery

    Boston, Massachusetts, 02111, United States

More trials for these conditions

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