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Clinical Trials in Egypt / NCT07374536
Active, not recruiting Not applicable

Clinical and Radiographic Evaluation of Local Application of Melatonin on Postoperative Outcomes After Surgical Removal of Impacted Mandibular Third Molar

NCT07374536 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-09-01
Last updated
2026-07-13

Condition(s) studied

Impact Molar

Investigational drug(s) / intervention(s)

ControlMelatonin gel

Control: the extraction socket will be left empty followed by suture of the socket after extraction

Melatonin gel: 3 mg of melatonin into 2 ml of 2% hydroxyethyl cellulose gel will be packed into the socket after extraction

Study summary

Clinical and Radiographic Evaluation of Local Application of Melatonin on Postoperative Outcomes after Surgical Removal of Impacted Mandibular Third Molar: A Randomized Controlled Study

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: 1)Both genders are included. 2)Adult patients (18-40) years 3)Healthy American Society of Anesthesiologists ASA I Patients. 4)Patients with class I or II impacted lower third molars with position A or B. \- Exclusion Criteria: 1. Pregnant \& lactating women. 2. Smoker patients. 3. Patients with poor oral hygiene. 4. Patients with bad oral habits as bruxism. 5. Patients with periapical or peri coronal lesions. 6. Patients with aggressive gingivitis or periodontitis.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry Suez Canal University Ismailia Egypt

More Suez Canal University trials in Egypt

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07374536 on ClinicalTrials.gov ↗ ← All trials in Egypt