Completed NA INTERVENTIONAL 1-arm NCT04441333

Usability, Safety and Efficacy of AspivixTM

Usability, Safety and Efficacy of AspivixTM, an Atraumatic Innovative Uterine Cervical Traction Device: a Pilot Phase Followed by a Comparative Study (Pilot)

Sponsor: Aspivix SA

Conditions IUD Insertion

Interventions AspivixTM cervical vacuum tenaculum

Updated 5 times since 2020 Last updated: Dec 10, 2020 Started: Jul 1, 2020 Primary completion: Dec 2, 2020 Completion: Dec 2, 2020

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A NA clinical study on IUD Insertion, this trial is completed. The trial is conducted by Aspivix SA and has accumulated 5 data snapshots since 2020. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

5 versions recorded

Sep 2024 — Present [monthly]

Completed NA
Jul 2024 — Sep 2024 [monthly]

Completed NA
Jan 2021 — Jul 2024 [monthly]

Completed NA

Status: Recruiting → Completed
Aug 2020 — Jan 2021 [monthly]

Recruiting NA

Status: Not Yet Recruiting → Recruiting
Jul 2020 — Aug 2020 [monthly]

Not Yet Recruiting NA

First recorded

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Aspivix SA

Data source: Aspivix SA

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Lausanne, Switzerland