Effectiveness and Safety Evaluation of Aqueduct 100-device

Status unconfirmed · Not applicable

Conditions studied: Cervix Uteri Dilation

In brief

Evaluation of efficacy and safety of using Aqueduct -100 - Cervical Dilator Device, focusing on diagnostic or operative hysteroscopies.

Key facts

Study ID

NCT02959567

Run by

Aqueduct Medical Ltd

People needed

100

Starts

2016-11-01

Expected to finish

2017-10-01

Last updated by the study team

2016-11-09

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Subjects, females, 18 years of age or older.
• Subjects undergoing diagnostic or operative hysteroscopies
• Subjects willing to sign informed consent form.

You may not qualify if…

• Subjects younger than 18 years of age
• Subjects unwilling to sign the informed consent form
• Pregnancy

Where it is running

• Baptist Medical Arts Surgical Center, Gynecology Department — Miami, Florida, United States

Full record on ClinicalTrials.gov

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