Ignite Creation Date:
2024-05-06 @ 8:22 PM
Last Modification Date:
2024-10-26 @ 3:26 PM
Study NCT ID:
NCT06358963
Status:
ENROLLING_BY_INVITATION
Last Update Posted:
2024-04-17
First Post:
2024-03-26
Brief Title:
CoQ10 and Omega-3 as Adjuncts to Periodontal Therapy TAC of Saliva
Sponsor:
Amirhossein Farahmand
Organization:
Islamic Azad University Tehran
Study Overview
Official Title:
Comparative Evaluation of CoQ10 and Omega-3 as Adjuncts to Periodontal Therapy and Total Antioxidant Capacity of Saliva
Status:
ENROLLING_BY_INVITATION
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Comparative evaluation of CoQ10 and Omega-3 as adjuncts to periodontal therapy and total antioxidant capacity of saliva randomized Double-Blind Clinicalials
Detailed Description:
This study was designed as a blind randomized clinical trial to evaluate teh efficacy of Coq10 Omega-3 supplement on periodontal parameters in chronic periodontitis patients total antioxidant capacity in saliva after 2 months of administration75 patients to department of periodontics were selected from teh patients referred to Broujerd dental school of teh Islamic Azad University of Medical Sciences before commencing teh study several clinical periodontal parameters were evaluated including plaque index bleeding on probing gingival index probing depth and clinical attachment levelCAL in six different areas of teh tooth surface subsequently scaling and root planningSRP were performed and oral hygiene practices were improved for all participants Teh subjects were then randomly assigned to three groups Group A received 30 mg of CoQ10 Group B was given 200 mg of Omega-3 daily supplements and Group C did not receive any medication after teh two-month study period teh clinical periodontal parameters were reassessed Additionally to compare teh total antioxidant capacity in saliva before and after teh intake of these supplements as well as in patients who did not receive any medication 2 ml of non-stimulated saliva was collected from each participant at teh beginning and end of teh study for analysis using UV-spectrophotometric methods furthermore teh following criteria determined teh selection of eligible participants for this study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None