Stitch showdown: which knot eases wisdom tooth recovery?
NCT ID NCT07327762
First seen Jun 27, 2026 · Last updated Sep 02, 2026 · Updated 2 times
Summary
This study compares two stitching methods (locked vs unlocked knots) after impacted wisdom tooth removal. 60 healthy adults aged 18-45 will be randomly assigned to one technique. The goal is to see which method leads to less jaw stiffness (trismus) and facial swelling after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- suture knot technique (locked vs unlocked)
- What this could lead to
- If one technique works better, it could lead to less pain and faster recovery after wisdom tooth removal.
- What could go wrong
- This is a small, early-stage trial with only 60 people, so results may not apply to everyone. The difference between techniques may be small.
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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60 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Aug 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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Up to 45 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * • Healthy individuals * Gender: male and female * Age: 18-45 years * Mandibular third molar impaction all positions * Mandibular third molar impaction all classes Exclusion Criteria: * • Patients with ASA status III and above * Patients requiring multiple extractions in same appointment * Patients allergic to Lignocaine * Patients in whom adrenaline is contraindicated * Medically compromised individual such as those with poorly controlled diabetes, hypertension and pregnancy, etc.
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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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Watim Medical and Dental College
Rawalpindi, Pakistan, 46200, Pakistan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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