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NCT02313883 · ClinicalTrials.gov registry record · Phase 1

A Phase I/II Study to Evaluate the Safety and Efficacy of PerioSept® as Adjunct to SRP in Subjects With Periodontitis

A Phase 1 study, sponsored by Geistlich Pharma.

Completed
Registry status
Phase 1
Development phase
127
Enrollment target

NCT02313883: Completed Phase 1 study, sponsored by Geistlich Pharma.

NCT02313883 is a Phase 1 study that has completed, run by Geistlich Pharma. The registered enrollment target is 127 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (112% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02313883, a Phase 1 study, has completed, sponsored by Geistlich Pharma.

COMPLETED
Registry status
Phase 1
Development phase
127 participants
Enrollment target

Study Summary

A Pharmacokinetic Pilot followed by a Phase I/II, Blinded, Randomized, Controlled, Parallel Arm Trial to Evaluate the Safety, Tolerability and Efficacy of PerioSept® and Scaling and Root Planing in Subjects with Periodontitis

Primary Outcome

Hematology safety labs, Chem 14, urine analysis, ECG, treatment emergent adverse events, local irritation, patient reported pain, sensisitivity, burning stinging

Interventions

  • DRUG PerioSept(r)

Trial Details

FieldValue
Enrollment Target 127 participants
Start Date 2015-07
Est. Completion 2018-07-02
Phase Phase 1
Geistlich Pharma

5 total trials

What the finished NCT02313883 record still lists

NCT02313883 is an interventional study that assigns participants to a tested intervention. The registered 127 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (112% higher).

The record links to 0 conditions, and to 1 intervention - of which PerioSept(r) is the first listed.

NCT02313883 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02313883 about?

NCT02313883 is a clinical study titled "A Phase I/II Study to Evaluate the Safety and Efficacy of PerioSept® as Adjunct to SRP in Subjects With Periodontitis". A Pharmacokinetic Pilot followed by a Phase I/II, Blinded, Randomized, Controlled, Parallel Arm Trial to Evaluate the Safety, Tolerability and Efficacy of PerioSept® and Scaling and Root Planing in Subjects with Periodontitis

What is the current status of trial NCT02313883?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 127 participants. The study started on 2015-07. Estimated completion is 2018-07-02.

What interventions are being tested in trial NCT02313883?

The interventions under investigation include: PerioSept(r) (DRUG).

Who is sponsoring clinical trial NCT02313883?

This trial is sponsored by Geistlich Pharma, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02313883's enrollment target sits among peer trials

127 459th of 2000 higher than 1,540 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02313883, the US trial registry maintained by the National Library of Medicine. NCT02313883 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.