Extraction of Distoangular and Vertically Positioned Mandibular 3rd Molars
NCT ID: NCT05032989
Last Updated: 2021-09-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
128 participants
INTERVENTIONAL
2021-09-15
2022-06-30
Brief Summary
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METHOD:
Total 128 patients will be recruited and divided into 64 patients in each group (two groups) attending in Dr. inshrat ul ebad institute of oral health sciences, Ojha, fulfilling inclusion criteria and undergoing extraction of 3rd molars will be included in this study. The participant will be briefed about the nature and purpose of the study. They will be ensured that their information will be used for the study purpose only. Informed consent from the participants will be obtained. Complete history from the patients will be taken and pre-operative evaluation will be done by clinical (pain and swelling) and radiographical (angulation of the tooth) examination. All the patients would undergo extraction of 3rd molars via both either conventional surgical technique or the proposed technique in the study. Followup will be done after 3 days to evaluate the same post-operative variables (pain and swelling) after extraction of 3rd molar and both techniques will then be compared in terms of variables measured.
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Detailed Description
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Objective:
To compare the effectiveness of new technique using cow horn forcep with conventional surgical method among patients with vertical and distoangular lower third molar impactions requiring extraction.
Method:
Total 128 patients will be recruited and divided into 64 patients in each group (two groups) attending in Dr. inshrat ul ebad institute of oral health sciences, Ojha, fulfilling inclusion criteria and undergoing extraction of 3rd molars will be included in this study. The participant will be briefed about the nature and purpose of the study. They will be ensured that their information will be used for the study purpose only. Informed consent from the participants will be obtained. Complete history from the patients will be taken and pre-operative evaluation will be done by clinical (pain and swelling) and radiographical (angulation of the tooth) examination. All the patients would undergo extraction of 3rd molars via both either conventional surgical technique or the proposed technique in the study. Followup will be done after 3 days to evaluate the same post-operative variables (pain and swelling) after extraction of 3rd molar and both techniques will then be compared in terms of variables measured.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Extraction of distoangular and vertically positioned 3rd molar using cowhorn forcep
Extraction with new technique
Extraction of mandibular 3rd molar via Cowhorn forcep technique
Cowhorn forceps technique used to extract the tooth results in less post operative pain and swelling also it makes the extraction easier.
Extraction of distoangular and vertically positioned 3rd molar via conventional method
Extraction with the conventional technique
Extraction of mandibular 3rd molar via conventional technique
Conventional method of extraction uses dental elevator and forceps resulting in post operative pain and swellig.
Interventions
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Extraction of mandibular 3rd molar via Cowhorn forcep technique
Cowhorn forceps technique used to extract the tooth results in less post operative pain and swelling also it makes the extraction easier.
Extraction of mandibular 3rd molar via conventional technique
Conventional method of extraction uses dental elevator and forceps resulting in post operative pain and swellig.
Eligibility Criteria
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Inclusion Criteria
* Bilateral partially impacted or erupted mandibular 3rd molars
* Both male and female patients
* Teeth which can be extracted by Intra-alveolar method under local anaesthesia
* Ages 18-35years
Exclusion Criteria
* Patients that are medically compromised (systemic diseases)
* Teeth having radiographically evident large periapical changes (abscess/granuloma/cyst)
* Patients previously treated with radiotherapy or chemotherapy or both
* Carious mandibular 2nd molar or missing 1st molar
18 Years
35 Years
ALL
Yes
Sponsors
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Dow University of Health Sciences
OTHER
Responsible Party
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Syed Wajid Hasan
Postgraduate Trainee
Principal Investigators
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Syed Wajid Hasan, BDS
Role: PRINCIPAL_INVESTIGATOR
DUHS
Central Contacts
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Other Identifiers
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wajid001
Identifier Type: -
Identifier Source: org_study_id
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