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New treatment option for Apical Periodontitis
Official title Effect of Photobiomodulation on Pain and Healing of the Vertical Releasing Incision After Endodontic Microsurgery
ClinicalTrials.gov ID: NCT06574152
What this study is testing
- What it's testing
- The purpose of this study is to evaluate the effect of Photobiomodulation (PBM) in postoperative pain after endodontic microsurgery (EMS) in patients from the University of Texas Health Science Center at Houston, School of Dentistry Graduate Endodontic Clinic and to assess the soft tissue healing of the vertical releasing incision (VRI) after PBM
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- American Society of Anesthesiologists (ASA) I or II.
- At least one tooth will receive EMS.
- Flap design that includes at least one VRI (triangular, rectangular, papilla base or submarginal rectangular).
You likely can't join if
- ASA III or IV.
- Current heavy smokers (\>10 cigarettes/day)
- Uncontrolled diabetes (HbA1c ≥ 7%) or other uncontrolled systemic diseases that may comprise healing, such as vitamin C deficiency, neutrophil...
- Surgical access on the palatal surface.
- Acute swelling or abscess present on the day of the surgery.
- Any event or condition that would make continued participation in the study not in the best interest of the subject, as determined by the...
See the full eligibility criteria
- American Society of Anesthesiologists (ASA) I or II.
- At least one tooth will receive EMS.
- Flap design that includes at least one VRI (triangular, rectangular, papilla base or submarginal rectangular).
- ASA III or IV.
- Current heavy smokers (\>10 cigarettes/day)
- Uncontrolled diabetes (HbA1c ≥ 7%) or other uncontrolled systemic diseases that may comprise healing, such as vitamin C deficiency, neutrophil deficiencies, immunodeficiency syndromes, or leukemia.
- Surgical access on the palatal surface.
- Acute swelling or abscess present on the day of the surgery.
- Any event or condition that would make continued participation in the study not in the best interest of the subject, as determined by the investigator.
- Pregnancy.
- Development of any medical condition that might affect the treatment and clinical outcomes, as determined by the investigator.
- Initiation of any treatment or exposure that might affect therapy's healing, as determined by the investigator.
The study team makes the final eligibility decision.
Where it's taking place
- Houston, Texas, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Houston, Texas, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.