Gum fluid test could spot tooth nerve inflammation
NCT ID NCT07592455
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
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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
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36 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Dec 2025
- Lead sponsor
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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
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18 to 50 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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AinShams University
Cairo, Cairo Governorate, 12611, Egypt
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