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Porcine Membrane vs Bovine Wound Dressing in Human Tooth Extraction Sites

NCT05802602 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2026-02-11

No results posted yet for this study

Summary

The purpose of this study is to compare porcine collagen membrane and bovine collagen wound dressing in human tooth extraction sites. The outcomes measured will be soft tissue thickness changes as well as bone density changes.

Conditions

  • Wound Heal

Interventions

DEVICE

Porcine Collagen Membrane

Atraumatic tooth extraction with porcine collagen membrane placement

DEVICE

Bovine Collagen Dressing

Atraumatic tooth extraction with bovine collagen dressing placement

Sponsors & Collaborators

  • University of Nebraska

    lead OTHER

Principal Investigators

  • Amy C Killeen, DDS, MS · University of Nebraska

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-04-16
Primary Completion
2025-11-30
Completion
2025-11-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05802602 on ClinicalTrials.gov