Could a dab of antibiotic in the tooth socket dull post-extraction pain?
NCT ID NCT07738861
First seen Jul 31, 2026 · Last updated Sep 15, 2026 · Updated 6 times
Summary
This trial tests whether placing tetracycline directly into the tooth socket after removing a lower molar can reduce post-operative pain. About 74 adults needing a molar extraction will be randomly assigned to receive either the antibiotic or no extra treatment. Pain levels will be measured at 24 hours, 48 hours, and 7 days after surgery, along with how many painkillers each person needs.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Tetracycline (250 mg) mixed with sterile saline, placed directly into the extraction socket after mandibular molar removal
- What this could lead to
- If effective, this simple, low-cost approach could become a standard way to ease pain and speed recovery after molar extractions.
- What could go wrong
- This is a small, early-stage trial, and the benefit may be modest. Tetracycline is an antibiotic, so there is a small risk of allergic reaction or local irritation.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
74 people
The number who actually took part.
- Started
-
Jan 2026
- Expected to finish
-
Oct 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
-
18 to 60 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 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: * Adults aged 18 to 60 years. * Male and female participants * Patients requiring surgical extraction of a mandibular molar. * American Society of Anesthesiologists (ASA) Physical Status I or II * Able and willing to provide written informed consent and comply with study follow-up Exclusion Criteria: * Pregnant or lactating women. * Patients with systemic conditions that contraindicate oral surgery (e.g., uncontrolled diabetes mellitus or immunosuppressive disorders). * Current use of antibiotics or medications that may interfere with wound healing (e.g., anticoagulants or bisphosphonates). * Known allergy or hypersensitivity to tetracycline or related antibiotics. * Requirement for simultaneous extraction of adjacent teeth. * Presence of active oral infection, including pericoronitis, at the surgical site. * Severely compromised oral hygiene that may affect postoperative healing. * Individuals who are unable to cooperate with the study procedures or attend follow-up visits because of physical or cognitive impairment.
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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
-
CMH Lahore
Lahore, Pakistan
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