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OpenTrials
Completed

NCT Number: NCT04848259

Effect of Honey and Dexamethason on Extraction Healing

Natural honey and dexamethason will be given before impaction removal then postoperative complications will be evaluated

Completed

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Vision colleges

Jeddah, Saudi Arabia

About this study

Patient with impacted lower third molar will be selected to this study agording to agent applied preoperative. Group 1 will receive topical honey and Group 2 will receive IV dexamethason. After surgical removal of impacted tooth under local anesthesia postoperative pain mouth opening, and swelling will be evaluated

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • impacted 3rd molar
  • healthy patient No smoking

Exclusion criteria

  • history of smoking Medical disease

Treatment and study plan

normal saline

Drug

Saline will be applied after surgery

Dexamethasone

Drug

Dexamethason will be given IV before surgery

Honey

Drug

Honey will be applied locally after surgery

Dexamethasone and honey

Drug

Dexamethason will be given IV before surgery and then Honey will be applied locally after surgery

Primary outcomes

  1. Interincisal distance

    Time frame: Preoperative

    Distance between upper and lower teeth will be measured in mm by ruler

  2. Interincisal distance

    Time frame: I day postoperative

    Distance between upper and lower teeth will be measured in mm by ruler

  3. Interincisal distance

    Time frame: 3rd day postoperative

    Distance between upper and lower teeth will be measured in mm by ruler

  4. Interincisal distance

    Time frame: 7th day postoperative

    Distance between upper and lower teeth will be measured in mm by ruler

  5. Edema

    Time frame: Preoperative

    Measured from angle of mandible to angle of mouth

  6. Edema

    Time frame: 1day postoperative

    Measured from angle of mandible to angle of mouth

  7. Edema

    Time frame: 2nd day postoperative

    Measured from angle of mandible to angle of mouth in mm by ruler

  8. Edema

    Time frame: 3rd day postoperative

    Measured from angle of mandible to angle hof mouth in mm by ruler

  9. Edema

    Time frame: 7th day postoperative

    Measured from angle of mandible to angle of mouth in mm by ruler

Sponsors and collaborators

Lead sponsor

Al-Azhar University

Other

Registry information

Official study title

A Novel Therapeutic Approach for Controlling Complications Associated With Impacted Mandibular Third Molar Removal

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Apr 19, 2021
Registry last updated
Jul 22, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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