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New study examines comfort and recovery after Full-Arch dental implants
NCT ID NCT07462598
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at how satisfied patients were and how much pain they felt after getting All-on-Four dental implants under sedation. 30 adults were followed for three days after surgery. Researchers measured pain, swelling, and how much pain medicine they used. The goal was to understand how well sedation works for this type of dental procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dental implant surgery under sedation
- What this could lead to
- If successful, this could help dentists improve comfort and pain management for patients getting full-arch dental implants.
- What could go wrong
- This is a small, completed study with only 30 participants. Results may not apply to everyone, and it only looked at short-term outcomes.
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.
- Participants
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30 people
The number who actually took part.
- Started
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Jan 2026
- Finished
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Apr 2026
- 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.
Who is studied
This prospective clinical study will include 30 patients classified as ASA physical status I-II who need to underwent full-arch rehabilitation using the All-on-Four implant concept
- Ages
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30 years and older
- 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: * Adult patients scheduled for elective full-arch implant rehabilitation * ASA physical status I or II * Ability to understand the study procedures and provide written informed consent Exclusion Criteria: * Emergency dental or surgical intervention * Pregnancy * Patients with cognitive impairment or psychiatric conditions affecting reliable outcome reporting * Patients with contraindications to analgo-sedation
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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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Dental Center, St.Caherine Hospital
Zagreb, Croatia