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Completed

NCT Number: NCT02071199

Treatment of Human Gingivitis With Amnion-derived Cellular Cytokine Solution (ACCS)

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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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Forsyth Institute

Boston, Massachusetts, 02142, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • good general health
  • ages 18-70 years
  • minimum of 20 natural teeth
  • modified gingival index score of 2.0 or greater and >40 percent bleeding sites at initial presentation.

Exclusion criteria

  • presence of orthodontic appliance
  • soft or hard tissue tumor of the oral cavity
  • carious lesion requiring immediate treatment
  • participation in another clinical trial within 30 days
  • pregnant or breast-feeding women
  • women of child-bearing potential refusing to use an acceptable method of birth control
  • antibiotic therapy within the last 30 days
  • chronic use (> 3 times/week) of non-steroidal anti-inflammatory medications (NSAID). Any use of steroids. Low dose (<325 mg) aspirin is allowed.
  • immune-compromised subjects
  • subjects with liver or kidney dysfunction on blood tests as evidenced by a value equal to or greater than 2X the upper limit of normal.
  • any medical history or any concomitant medication that might affect the assessment of the study treatment or periodontal tissues such as diabetes rheumatoid arthritis, Crohn's disease, use of nifedipine, phenytoin (Dilantin), anticoagulant medications (e.g. warfarin), ongoing cancer treatment either with radiation of chemotherapy.

Treatment and study plan

1X ACCS (Amnion-derived Cellular Cytokine Solution)

Drug

1X ACCS will be applied to the gingival margin daily 5 days per week for 2 weeks

Other names: ACCS

normal saline

Drug

Saline will be applied to the gingival margin daily 5 days per week for 2 weeks

Other names: saline placebo

0.3X ACCS

Drug

0.3X ACCS will be applied to the gingival margin daily 5 days per week for 2 weeks

Other names: Diluted ACCS

Primary outcomes

  1. Incidence of adverse/serious adverse events

    Time frame: End of two weeks of treatment and at two weeks follow-up visit

Secondary outcomes

  1. Probing pocket depth

    Time frame: Bseline and after two weeks of treatment

    Depth will be measured at six sites per tooth

  2. Modified gingival index

    Time frame: Baseline and after two weeks of treatment

    Gingival index will be measured at six sites per tooth

  3. Bleeding on probing

    Time frame: Baseline and after two weeks of treatment

    Bleeding will be measured at six sites per tooth

  4. Plaque index

    Time frame: Baseline and after two weeks of treatment

    Only the gingival third of the tooth will be evaluated

  5. Microbial analysis

    Time frame: Baseline and after two weeks of treatment

    6 teeth will be sampled

  6. Cytokine analysis

    Time frame: Baseline and after two weeks of therapy

    Inflammatory cytokines will be sampled in crevicular fluid

Sponsors and collaborators

Lead sponsor

Noveome Biotherapeutics, formerly Stemnion

Industry

Registry information

Official study title

Treatment of Human Gingivitis With Topical ACCS: a Two Week Safety Dose-ranging and Proof-of-principle Trial

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Feb 25, 2014
Registry last updated
Nov 29, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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