Evaluation of the Nella Women's Care Line

NCT03123367 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 154

Last updated 2018-03-16

No results posted yet for this study

Summary

Evaluation of the Nella Women's Care Line

Conditions

  • GYN Disorders

Interventions

DEVICE

Group 1: Nella VuSleeve

Sleeve

DEVICE

Group 2: Nella NuSpec

Speculum

DEVICE

Group 3: NellaSpec

Speculum

DEVICE

Group 4: Nella Insert

Sleeve

Sponsors & Collaborators

  • Ceek Enterprises

    lead INDUSTRY

Principal Investigators

  • Ceek Clinical Research · Ceek Enterprises

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-06
Primary Completion
2017-06-27
Completion
2017-06-27
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 NCT03123367 on ClinicalTrials.gov