- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01780493
The Long Term Follow-Up Results Of The Direct Nipple Ureteroneocystostomy Technique
January 30, 2013 updated by: Abdullah Demirtas, TC Erciyes University
The Long Term Follow-Up Results Of The Direct Nipple Ureteroneocystostomy Technique: A Prospective Study
To evaluate the long term follow-up results of the direct nipple ureteroneocystostomy technique.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
19
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Kayseri, Turkey, 38039
- Erciyes University Medical Faculty, Department of Urology
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Megaureter.
- Ligated Ureter during surgery.
Exclusion Criteria:
- Neurogenic bladder
- Surgical wound infection
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Direct Nipple Ureteroneocystostomy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Inter-IVU image differences and DMSA uptakes
Time Frame: 3 month after surgery
|
In cases attending regular follow-ups, preoperative and postoperative 1st year DMSA results and amount of pelvicaliceal dilatation in the IVU of the unit that underwent surgery were compared statistically (by counting the dots falling on the pelvis and calices using stereologic methods which use transparent acetates with 3-mm inter-grid distances.
Inter-IVU image differences between IVUs taken at different centers were resolved by using the value found by counting the dots falling on the 4th lumbar vertebra in both films and proportioning the results with each other as the multiplier.
Measurable values were expressed as means + standard deviation.
|
3 month after surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2004
Primary Completion (Actual)
February 1, 2008
Study Completion (Actual)
August 1, 2011
Study Registration Dates
First Submitted
January 22, 2013
First Submitted That Met QC Criteria
January 30, 2013
First Posted (Estimate)
January 31, 2013
Study Record Updates
Last Update Posted (Estimate)
January 31, 2013
Last Update Submitted That Met QC Criteria
January 30, 2013
Last Verified
January 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 03.04.2007/172
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Vesicoureteral Reflux
-
St. Luke's Medical Center, PhilippinesCompletedUrinary Tract Infection | Vesicoureteral Reflux (VUR)Philippines
-
Centre Hospitalier Universitaire de NīmesRecruiting
-
Johns Hopkins UniversityTerminatedVesicoureteral RefluxUnited States
-
Stanford UniversityLucile Packard Children's HospitalCompleted
-
Stanford UniversityCompletedVesicoureteral RefluxUnited States
-
Washington University School of MedicineSociety of Pediatric UrologyTerminatedVesicoureteral RefluxUnited States
-
Connecticut Children's Medical CenterCompleted
-
Boston Children's HospitalWithdrawnVesicoureteral RefluxUnited States
-
Samsung Medical CenterCompletedVesicoureteral RefluxKorea, Republic of
-
University of AlbertaCanadian Urological AssociationWithdrawn
Clinical Trials on The Direct Nipple Ureteroneocystostomy Technique
-
Centre Hospitalier Universitaire, AmiensWithdrawn
-
Sunnybrook Health Sciences CentreRecruitingRhegmatogenous Retinal DetachmentCanada
-
Damascus UniversitySt Joseph University, Beirut, Lebanon; Syrian Atomic Energy Agency, Damascus...CompletedImplant Site ReactionLebanon, Syrian Arab Republic
-
Cairo UniversityNot yet recruitingEndodontically Treated Teeth
-
Beijing Friendship HospitalBeijing Health Promotion AssociationRecruitingStage I Breast Cancer | Stage II Breast CancerChina
-
Prince of Songkla UniversityCompletedAngle Closure GlaucomaThailand
-
University of ValenciaCompleted
-
Ondokuz Mayıs UniversityActive, not recruitingAnesthesia | AirwayTurkey
-
Washington University School of MedicineCompletedCommunication | Behavior and Behavior MechanismsUnited States