Viewing Study NCT00757432


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Study NCT ID: NCT00757432
Status: COMPLETED
Last Update Posted: 2011-04-11
First Post: 2008-09-19
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Recovery After Robotic Urogynecological Surgery: The Patient's Perspective
Sponsor: University of Rochester
Organization:

Study Overview

Official Title: Recovery After Robotic Urogynecological Surgery: The Patient's Perspective
Status: COMPLETED
Status Verified Date: 2011-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of the study is to describe the patient experience, including pain scores, use of pain medications, resumption of usual activities, and bowel function in the post-operative period following robotic urogynecologic surgery. Additionally, to describe peri-operative parameters of robot-assisted urogynecologic surgery.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: