Shockwave Lithotripsy (SWL) Under Selective, General Anesthesia.

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2009 by Assaf-Harofeh Medical Center.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by:
Assaf-Harofeh Medical Center
ClinicalTrials.gov Identifier:
NCT01008267
First received: November 4, 2009
Last updated: NA
Last verified: March 2009
History: No changes posted
  Purpose

SWL is widely used in the treatment of patients with renal and ureteral calculi. Several factors determine the success of extracorporeal shockwave lithotripsy (SWL) for kidney stones: stone size, stone location within the collecting system, stone type, and the SWL machine used. Moreover, in some cases it is very difficult to focus on the stone because of its movement as a results of breathing. In order to prevent stone movement we want to use a bronchial blocker, processing a selective ventilation of the opposite side of stone location.


Condition
Renal Calculi
Ureteral Calculi

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Shockwave Lithotripsy (SWL) Under Regular General Anesthesia and Under General Anesthesia Using Bronchial Blocker.

Further study details as provided by Assaf-Harofeh Medical Center:

Estimated Enrollment: 60
Study Start Date: November 2009
Estimated Primary Completion Date: October 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts
SWL under general anesthesia
Patients who failed in SWL under sedation(a standard protocol), will undergo a second SWL process under general anesthesia.
SWL under general selective anesthesia
Patients who failed in SWL under sedation(a standard protocol), will undergo a second SWL process under general selective anesthesia, using a bronchial blocker.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients who failed in SWL process taken under sedation (standard protocol)

Criteria

Inclusion Criteria:

  • Older than 18 years old
  • Not pregnant
  • All patients who failed in SWL process, taken under sedation (standard protocol)

Exclusion Criteria:

  • Age < 18
  • Pregnancy
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01008267

Locations
Israel
Anesthesiology department, Assaf-Harofeh MC Not yet recruiting
Beer-Yaakov, Zrifin, Israel, 70300
Contact: Zoya Haitov, MD    089778080    ZoyaC@asaf.health.gov.il   
Principal Investigator: Zoya Haitov, MD         
Sponsors and Collaborators
Assaf-Harofeh Medical Center
  More Information

No publications provided

Responsible Party: Zoya Haitov MD, Anesthesiology department, Assaf-Harofeh Medical Center
ClinicalTrials.gov Identifier: NCT01008267     History of Changes
Other Study ID Numbers: 63/09
Study First Received: November 4, 2009
Last Updated: November 4, 2009
Health Authority: Israel: Ministry of Health

Additional relevant MeSH terms:
Ureteral Diseases
Calculi
Kidney Calculi
Ureteral Calculi
Ureterolithiasis
Pathological Conditions, Anatomical
Nephrolithiasis
Kidney Diseases
Urologic Diseases
Urolithiasis
Urinary Calculi
Anesthetics
Central Nervous System Depressants
Physiological Effects of Drugs
Pharmacologic Actions
Central Nervous System Agents
Therapeutic Uses

ClinicalTrials.gov processed this record on September 18, 2014