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

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Numbing shot through the nose could soothe sore throats after surgery

NCT ID NCT07370129

Symptom relief Sponsor: Ankara 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a numbing medicine (lidocaine) applied to a nerve cluster in the nose can reduce pain after tonsillectomy. Twenty-eight patients will receive either lidocaine or a placebo before surgery. Researchers will track pain levels, painkiller use, and recovery for 14 days after the operation.

What this could mean

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

Active substance
lidocaine
What this could lead to
If it works, this could offer a simple way to ease pain after tonsillectomy and reduce the need for strong painkillers.
What could go wrong
This is a very small, early-stage trial with only 28 participants. The results may not apply to everyone, and the block might not work better than 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.

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 28 people

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

Started

Jun 2025

Expected to finish

Jun 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

12 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: * Patients aged ≥ 12 years * Patients weighing ≥ 50 kg * Patients without coagulation disorders * ASA physical status I-II patients scheduled for tonsillectomy * Patients who are fully oriented and able to cooperate Exclusion Criteria: * Lack of informed consent * Patients aged \< 12 years * Patients weighing \< 50 kg * Body mass index (BMI) \> 30 kg/m² * History of allergy to local anesthetics * History of facial trauma or infection * Presence of coagulation disorders * Patients who are disoriented and/or unable to cooperate * Patients with comorbidities requiring opioid use * History of neuropathic pain * Patients with chronic pain syndrome

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Opioid consumption 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.

Opioid consumption Post operative analgesia Post-tonsillectomy pain Sphenopalatine ganglion block Tonsillar surgery complications

How to take part

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

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. 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.

Contacts and locations

Locations

  • Ankara University

    Ankara, Ankara, 06180, Turkey (Türkiye)

More trials for these conditions

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