Urodynamic Evaluation in Patients With Anorectal Malformation According to Spinal Cord Abnormalities

Anorectal Malformation Clinical Trial

Official title:

Urodynamic Evaluation in Patients With Anorectal Malformation According to Spinal Cord Abnormalities

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00909415
• Other study ID #: 4-2009-0171
• Status: Completed
• Phase: N/A
• First received: May 26, 2009
• Last updated: January 26, 2012
• Start date: May 2009
• Est. completion date: May 2011

Study information

• Verified date: January 2012
• Source: Yonsei University
• Contact: n/a
• Is FDA regulated: No
• Health authority: South Korea: Korea Food and Drug Administration (KFDA)
• Study type: Observational

Clinical Trial Summary

This study will examine the effects of spinal cord abnormalities on perioperative neurovesical dysfunction in patients with anorectal abnormalities.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 53
• Est. completion date: May 2011
• Est. primary completion date: May 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 1 Month to 11 Years

Eligibility

Inclusion Criteria:

• Anorectal malformation patients who underwent preoperative and postoperative urodynamic studies

Exclusion Criteria:

• Severe artifacts in urodynamic result graph when the postoperative urodynamic study was done after spinal surgery

Study Design

Time Perspective: Retrospective

Related Conditions & MeSH terms

• Anorectal Malformation
• Congenital Abnormalities

Locations

Country	Name	City	State
Korea, Republic of	Severance Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of,