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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04424875
Other study ID # Melatonin and 3rd molar
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date July 1, 2020
Est. completion date May 1, 2021

Study information

Verified date May 2021
Source Fayoum University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In the present study, the main hypothesis hypothesizes that the local application of melatonin in the post-extraction socket produces favorable differences in the immediate postoperative period, as anti-inflammatory, analgesic, and early osteogenic regarding the natural healing process of the socket.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date May 1, 2021
Est. primary completion date March 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age =18ys - no systemic disease - impacted mandibular third molar class II position B on Pell- Gregory classification Exclusion Criteria: - history of metabolic or systemic diseases affecting bone or healing process, - local infection, - tobacco use, - oral contraceptive, - pregnancy and lactation - patients who had taken analgesics or anti-inflammatories for 1 week prior to enrollment in the study

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
3 mg melatonin
patients will remove impacted third molar and receive 3 mg melatonin into 2 ml hydroxyethyl cellulose gel 2%
Placebo
patients will remove impacted third molar and receive 2 ml hydroxyethyl cellulose gel 2%

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Fayoum University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Cobo-Vázquez C, Fernández-Tresguerres I, Ortega-Aranegui R, López-Quiles J. Effects of local melatonin application on post-extraction sockets after third molar surgery. A pilot study. Med Oral Patol Oral Cir Bucal. 2014 Nov 1;19(6):e628-33. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Bone density The bone density within the extraction socket was measured using software of cone beam 6months
Secondary Osteoprotegerin (OPG) Human Osteoprotegerin (OPG) ELISA Kit was used to detect OPG levels.The changes in OPG in the whole group in the predetermined period immediate postoperative , after 4 week,and 6months 4weeks postoperatively
Secondary pain sensation a visual analogue scale (VAS) of 10 units in combination with a graphic rating scale. On the VAS, the left most end represented the absence of pain (score 0) and the right most end indicated the most severe pain (score 10). 7 days postoperative
Secondary swelling a tape measure, from the tragus to the corner of the mouth. 7 days postoperative
Secondary trismus measuring the distance between incisal edges of upper and lower central incisor at maximal mouth 7days postoperative
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