Clinical Trials Directory

Trials / Completed

CompletedNCT01442818

Patient Satisfaction and Pain Control Following Reconstructive Vaginal Surgery

Patient Satisfaction and Pain Control Following Reconstructive Vaginal Surgery: A Randomized Trial Comparing Patient-Controlled Intravenous Analgesia (PCA) to Scheduled Intravenous Analgesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
54 (actual)
Sponsor
TriHealth Inc. · Academic / Other
Sex
Female
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The investigators hypothesize that patient controlled analgesia (PCA) provides superior pain relief and patient satisfaction when compared to scheduled intravenous analgesia following vaginal reconstructive surgery.

Detailed description

The investigators hypothesize that patient controlled analgesia (PCA) provides superior pain relief and patient satisfaction when compared to scheduled intravenous analgesia following vaginal reconstructive surgery. In order to determine if there is a significant correlation, secondary outcomes will include the daily and total narcotic volume used, common side effects from the opioid including nausea, vomiting, or pruritis, length of hospital stay, timing of flatus and first bowel movement, all complications, and procedure performed.

Conditions

Interventions

TypeNameDescription
DRUGDilaudid PCAPCA setting of 0.3mg demand dose, 8 minute lock out interval, and 5mg 4-hour limit.
DRUGDilaudid IV ScheduledNurse administered IV Dilaudid 0.5mg every 2 hours.

Timeline

Start date
2010-09-01
Primary completion
2011-09-01
Completion
2012-10-01
First posted
2011-09-29
Last updated
2015-07-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01442818. Inclusion in this directory is not an endorsement.

Patient Satisfaction and Pain Control Following Reconstructive Vaginal Surgery (NCT01442818) · Clinical Trials Directory