Forsyth Institute
Boston, Massachusetts, 02142, United States
NCT Number: NCT02071199
The purpose of this study is to evaluate the safety of oral topical application of Amnion-derived Cellular Cytokine Solution (ACCS) in subjects with gingivitis
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Notify Me18 year–70 year
All sexes
Interventional
Phase 1
Boston, Massachusetts, 02142, United States
This randomized blinded study will evaluate the use of ACCS in subjects with gingivitis. Two doses of ACCS will be used. It will be given topically intra-orally daily Monday through Friday for 2 weeks. In the first cohort, a low dose of ACCS or saline will be given by random chance. If there are no safety issues, cohort two will include a higher dose of ACCS randomized with saline. Pocket depth, plaque index, gingival index, and bleeding on probing will be assessed. To assess shifts in supragingival flora, a qualitative and quantitative microbial analysis will be performed for common oral bacteria. There will also be an analysis of inflammatory cytokines in crevicular fluid at the beginning and end of the study. Comparisons of adverse events and outcomes will be made between the subjects receiving low dose ACCS, high dose ACCS, and saline.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1X ACCS will be applied to the gingival margin daily 5 days per week for 2 weeks
Other names: ACCS
Saline will be applied to the gingival margin daily 5 days per week for 2 weeks
Other names: saline placebo
0.3X ACCS will be applied to the gingival margin daily 5 days per week for 2 weeks
Other names: Diluted ACCS
Time frame: End of two weeks of treatment and at two weeks follow-up visit
Time frame: Bseline and after two weeks of treatment
Depth will be measured at six sites per tooth
Time frame: Baseline and after two weeks of treatment
Gingival index will be measured at six sites per tooth
Time frame: Baseline and after two weeks of treatment
Bleeding will be measured at six sites per tooth
Time frame: Baseline and after two weeks of treatment
Only the gingival third of the tooth will be evaluated
Time frame: Baseline and after two weeks of treatment
6 teeth will be sampled
Time frame: Baseline and after two weeks of therapy
Inflammatory cytokines will be sampled in crevicular fluid
Noveome Biotherapeutics, formerly Stemnion
Industry
Treatment of Human Gingivitis With Topical ACCS: a Two Week Safety Dose-ranging and Proof-of-principle Trial
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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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