NCT Number: NCT00534963
Optimal Catheter Placement During Sonohysterography: Comparison of Cervical to Uterine Placement
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.
Looking for future studies?
Notify MeKey information
Conditions
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
About this study
The use of sonography combined with intrauterine saline instillation, termed sonohysterography
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Female patients undergoing SIS for diagnostic uterine cavity evaluation at our university's Reproductive Endocrine Infertility Program.
Exclusion criteria
- previous hysterectomy, current pregnancy, active PID, patulous or stenotic cervical os noted on previous history or physical exam.
Treatment and study plan
Primary outcomes
-
Measure: perceived discomfort
Time frame: during sonohysterography procedure
Secondary outcomes
-
Measure: Time required to perform procedure; Measure: Volume of media required to perform procedure
Time frame: during sonohysterography procedure
Sponsors and collaborators
Lead sponsor
University of Wisconsin, Madison
Other
Registry information
Official study title
Optimal Catheter Placement During Sonohysterography: A Randomized Clinical Trial Comparing Cervical to Uterine Placement
Important dates
- Study start
- 2004
- Study completion
- 2005
- First posted
- Sep 26, 2007
- Registry last updated
- Oct 26, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Effect Of Local Cold Applıcatıon On Paın and Vıtal Sıgns Durıng Port Catheter Needle Insertıon
NCT06816420
Catheter Placement and Perceived Pain, Neurologic Manifestations
Konya, Meram, Turkey (Türkiye)
View Trial Details