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Clinical trialNCT00979342CompletedInterventional

Comparative Sedation Study of the MyoSure Hysteroscopic Tissue Removal System

SponsorHologic, Inc.Enrollment40PolypsUterine Fibroids
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to develop a recommended local anesthetic protocol and post-treatment pain management regimen, in order to assure patient comfort during office-based treatment with the MyoSure Hysteroscopic Tissue Removal Device. Subject self-reported pain scores (as rated on an 11 point scale) will be compared at multiple time intervals between all treatment groups.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

5 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Phoenix Gynecology Consultants

    Phoenix, Arizona, United States

  • Florida Woman Care

    Boca Raton, Florida, United States

  • Wayne State University

    Detroit, Michigan, United States

  • Minnesota Gynecology and Surgery

    Edina, Minnesota, United States

  • Carolina Women'S Research and Wellness Center

    Durham, North Carolina, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Nov 2009
Primary completion
31 Jul 2010
Completion
31 Jul 2010
Last update posted
23 Jul 2010
Registered enrollment
40
Registry id
NCT00979342

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.