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Evaluation of Pain During Hysterosalpingography With The Use Of Balloon Catheter Versus Metal Cannula

NCT02020733 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 194

Last updated 2013-12-25

No results posted yet for this study

Summary

The aim of this study is to compare the metal cannula routinely used in our clinical practice with intrauterine hysterosalpingography catheter as a probable alternative device in a prospective, single-blinded, randomized study.

Conditions

  • Pain During Hysterosalpingography

Interventions

DEVICE

Balloon catheter

DEVICE

metal cannula

Sponsors & Collaborators

  • Sadiman Kiykac Altinbas

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2013-02-28
Completion
2013-02-28

Countries

  • Turkey (Türkiye)

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 NCT02020733 on ClinicalTrials.gov