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Optimal Catheter Placement During Sonohysterography: Comparison of Cervical to Uterine Placement

NCT00534963 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 69

Last updated 2017-10-26

No results posted yet for this study

Summary

The primary objective of this investigation was to evaluate if the location of placement of the SIS balloon into either the uterine cavity or the cervical canal affected discomfort perceived during the examination.

Conditions

  • Catheter Placement and Perceived Pain

Interventions

PROCEDURE

cervical vs. uterine placement of balloon catheter

Sponsors & Collaborators

  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • Steven Lindheim, MD · University of Wisconsin Department of Reproductive Endocrinology and Infertility

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2004-12-31
Completion
2005-08-31

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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 NCT00534963 on ClinicalTrials.gov