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Gum fluid test could spot tooth nerve inflammation

NCT ID NCT07592455

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study looked at 36 adults with painful tooth nerve inflammation (irreversible pulpitis) to see if biological markers in gum fluid match symptoms. Researchers collected gum fluid samples before and after root canal treatment and measured pain levels. The goal was to find a link between clinical signs and substances like TNF-alpha and substance P in the inflamed tissue.

What this could mean

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

What this could lead to
If successful, this could help dentists diagnose tooth nerve inflammation more accurately using simple gum fluid tests.
What could go wrong
This is a small, completed observational study with only 36 participants. Results may not apply to all patients or lead to immediate clinical changes.

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

36 people

The number who actually took part.

Started

Sep 2025

Finished

Dec 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 to 50 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 Systemically healthy male and female individuals aged between 18 and 50 years No physical or mental disabilities No underlying systemic diseases Mandibular permanent premolar teeth diagnosed with symptomatic irreversible pulpitis with apical periodontitis Mandibular permanent premolar teeth diagnosed with symptomatic irreversible pulpitis without apical periodontitis Diagnosis based on the terminology of the American Association of Endodontists (2009) Patients who provided written informed consent Fully developed teeth with no previous pulp exposure Positive response to cold testing Positive response to electric pulp testing Exclusion Criteria Requirement for antibiotic prophylaxis Diabetes or hematologic disorders Use of anti-inflammatory drugs, antibiotics, or antidepressants within the previous four weeks Pregnancy at the time of treatment Heavy plaque or calculus accumulation Gingival redness and bleeding Severe gingivitis or generalized periodontitis Gingival pocket depths greater than 3 mm Negative response to sensibility testing (cold test or electric pulp testing) Presence of apical radiolucency (PAI \> 2) Previously initiated endodontic treatment Internal or external root resorption History of trauma Severe calcific metamorphosis with obliterated root canal spaces on periapical radiographs Vertical root fractures Mobility greater than Grade I (Miller's mobility index) Swelling or sinus tract associated with the treated tooth Presence of periodontal-endodontic lesions Teeth that could not be properly isolated with a dental dam Collection of less than 10 µL of blood from each site Conflicting clinical and radiographic findings preventing clear group assignment No bleeding from one or more canal orifices (possible partial necrosis)

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Conditions

The condition(s) this trial relates to.

pulpitis Toothache

As listed by the trial registrant

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

Contacts and locations

Locations

  • AinShams University

    Cairo, Cairo Governorate, 12611, Egypt

More trials for these conditions

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