World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 October 2017
Main ID:  NCT01195116
Date of registration: 13/08/2010
Prospective Registration: No
Primary sponsor: University of Rochester
Public title: Usefulness of Dexmedetomidine on Post-operative Pain Management in Patients With Interstitial Cystitis
Scientific title: Usefulness of Dexmedetomidine on Post-operative Pain Management in Patients With Interstitial Cystitis
Date of first enrolment: May 2010
Target sample size: 41
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT01195116
Study type:  Interventional
Study design:   
Phase:  Phase 4
Countries of recruitment
United States
Contacts
Name:     Suzanne Karan, MD
Address: 
Telephone:
Email:
Affiliation:  University of Rochester Department of Affiliation
Name:     Robert Mayer, MD
Address: 
Telephone:
Email:
Affiliation:  University of Rochester Department of Urology
Name:     Denham Ward, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  University of Rochester Department of Anesthesiology
Key inclusion & exclusion criteria

Inclusion Criteria:

- Patients with a clinical diagnosis of IC scheduled for cystoscopy and hydrodistension
for both diagnostic and therapeutic indications.

- 2. Gender of Patients: Male & female,Age of Patients: 18 and older

Exclusion Criteria:

- Conduction disturbance (second degree AV block or greater), or previous reaction to
medications used in this study. Patients receiving spinal anesthesia will not be
included.



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Interstitial Cystitis
Intervention(s)
Drug: Normal Saline
Drug: Dexmedetomidine
Primary Outcome(s)
Change in Pain Score (1-10, 10 is Most Pain) From Baseline, to Average Post op Pain Score in PACU [Time Frame: Assessed every 15 minutes while in Post Anesthesia Care Unit until discharged home, which was approximately 10 times on the average]
Secondary Outcome(s)
Secondary ID(s)
RSRB 31154
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available: Yes
Date Posted: 24/03/2015
Date Completed:
URL: https://clinicaltrials.gov/ct2/show/results/NCT01195116
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history