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Search / Trial NCT06435832

Evaluations of the Effects of Tranexamic Acid and Chlorhexidine Gel on Alveolar Osteitis Incidence

Launched by RECEP TAYYIP ERDOGAN UNIVERSITY · May 24, 2024

Trial Information

Current as of May 18, 2025

Active, not recruiting

Keywords

Alveolar Osteitis

ClinConnect Summary

This clinical trial is studying the effects of two different treatments—tranexamic acid and chlorhexidine gel—on a condition called alveolar osteitis, which can occur after a tooth extraction. Alveolar osteitis, also known as dry socket, happens when the blood clot that forms in the empty tooth socket becomes dislodged or does not form properly, leading to pain and other complications. The trial involves healthy adults aged 18 to 65 who need molar or premolar teeth extracted. Participants will be randomly assigned to receive one of three treatments after their tooth extraction: a special sponge, a sponge with chlorhexidine gel, or a sponge with tranexamic acid.

During the trial, participants can expect to visit the clinic for check-ups on the 3rd and 7th days after their extraction, where their pain and swelling will be assessed using a simple scale from 0 to 10. The researchers will also look for signs of complications, such as bad breath or difficulty opening the mouth. It’s important to note that people with certain allergies, recent infections, or other specific health conditions cannot participate in this study. This trial is ongoing and is not currently recruiting new participants.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Healthy individuals between the ages of 18-65
  • 2. Molar and premolar teeth with extraction indication
  • Exclusion Criteria:
  • 1. Against drugs or substances to be used in surgery (articaine, tranexamic acid, chlorhexidine) have allergies,
  • 2. Those who used antibiotics 30 days before the dental extraction,
  • 3. Clinical and radiological examinations in the operation area 30 days before dental extraction and/or on the day of the procedure.
  • Any signs of pathology and infection (such as periapical pathology, pericoronitis),
  • 4. Those who routinely use oral antiseptics,
  • 5. Systemic fever, absence of growth such as lymphadenopathy (LAP),
  • 6. Women are lactating or pregnant,
  • 7. Using oral contraceptives,
  • 8. Procedures that were not attended to control appointments (day 3-7) were not included.

About Recep Tayyip Erdogan University

Recep Tayyip Erdogan University is a prominent academic institution committed to advancing healthcare through innovative research and clinical trials. Located in Turkey, the university fosters a collaborative environment that integrates cutting-edge science with clinical practice. With a focus on enhancing patient care and contributing to medical knowledge, the university actively engages in diverse clinical research initiatives aimed at addressing pressing health challenges. Its multidisciplinary approach ensures rigorous study design and ethical standards, positioning the institution as a key player in the advancement of medical research and education in the region.

Locations

Rize, , Turkey

Patients applied

0 patients applied

Trial Officials

Zeynep Gümrükçü

Study Director

Recep Tayyip Erdogan University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported