Laparoscopic Versus Open Partial Nephrectomy - Surgical and Oncological Outcomes (LapVsOpen prtn)
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: Shay Golan, MD
- Phone Number: 972-50-7447573
- Email: shaygo1@yahoo.com
Study Locations
-
-
-
Petach Tikva, Israel
- Recruiting
- Rabin Medical Center
-
Contact:
- shay golan, MD
- Phone Number: 972-50-3447573
- Email: shaygo1@yahoo.com
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients referred to partial nephrectomy
Exclusion Criteria:
- Contra-indication for laparocopic surgery
- Complexed , large tumors, single kidney, chronic renal failure
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Number of groups / cohorts
Cohorts and Interventions
Group / CohortGroup / Cohort |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Laparoscopic partial nephrectomy
|
Laparoscopic partial nephrectomy
|
|
Open Partial nephrectomy
|
Open partial nephrectomy
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion
Primary Completion
Study Completion
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- 5489
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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