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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05850650
Other study ID # REU
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date May 1, 2023
Est. completion date November 15, 2023

Study information

Verified date April 2023
Source Riyadh Colleges of Dentistry and Pharmacy
Contact Nedal A Abu-Mostafa, Assistant P
Phone 00966506275782
Email nabumostafa@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this randomized controlled trial is to compare pain, mouth opening, and alveolar osteitis following surgical extraction of bilateral symmetrical impacted lower third molars using two types of wound closures. Collagen plugs will be applied in the sockets of the study side followed by suture, while the controlled side will be sutured without a collagen plug. The study will include 40 patients aged between 18- 40 years old, medically fit (ASA1), who have bilateral symmetrical impacted lower third molars and visit the oral surgery clinics of King Saud Medical City for extraction. The main question is" Does intra-alveolar collagen application after surgical extraction of impacted lower third molars reduce the incidence of alveolar osteitis?


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date November 15, 2023
Est. primary completion date October 15, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: Forty patients aged between 18- 40 years old, ASA1, who have bilateral symmetrical impacted lower third molars and visit the oral surgery clinics of King Saud Medical City for extraction. Exclusion Criteria: Uncontrolled systemic diseases, diabetes, bone diseases, smokers, epinephrine contraindications, pregnant women, breastfeeding women, and those who were using oral contraceptives. Other exclusion criteria are the presence of acute infection and facial swelling, cystic lesions, and TMJ problems. Moreover, any surgical extraction that lasts more than 30 minutes +/- 5 minutes, or has been done without the whole standardized steps will be excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Application of a collagen sponge after surgical extraction of impacted 3rd molar
Application of a collagen sponge after surgical extraction of impacted 3rd molar
No collagen sponge application after surgical extraction of impacted 3rd molar
No collagen sponge application after surgical extraction of impacted 3rd molar

Locations

Country Name City State
Saudi Arabia RiyadH Colleges of dentistry and Pharmacy Riyadh

Sponsors (1)

Lead Sponsor Collaborator
Riyadh Colleges of Dentistry and Pharmacy

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pre-extraction Pain score Pain measurement by VAS (0-10). 0: no pain. 10: worst pain Pre-extraction
Primary Pre-extraction Halitosis Halitosis in reported in the presence of a bad odor that is smelled by the investigator during the patient's speech Pre-extraction
Primary Pre-extraction Mouth opening Maximum Mouth opening is taken by a caliber Pre-extraction
Primary Pain score Day3 Pain measurement by VAS (0-10). 0: no pain. 10: worst pain 3 days after extraction
Primary Pain score Day7 Pain measurement by VAS (0-10). 0: no pain. 10: worst pain 7 days after extraction
Primary Mouth opening Day7 Maximum Mouth opening is taken by a caliber 7 days after extraction
Primary Halitosis Day7 Halitosis in reported in the presence of a bad odor that is smelled by the investigator during the patient's speech 7 days after extraction
Primary Alveolar osteitis is diagnosed if the patient complains of pain (more than 5) between day 2 and day 4 with empty sockets and food debris, with or without halitosis After 3 days of extraction
See also
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