We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Comparison Epidural Anesthesia and General Anesthesia in Laparoscopic Cholecystectomy

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified July 2011 by National Taiwan University Hospital.
Recruitment status was:  Enrolling by invitation
Sponsor:
ClinicalTrials.gov Identifier:
NCT01398683
First Posted: July 20, 2011
Last Update Posted: November 16, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
National Taiwan University Hospital
  Purpose
Comparison of epidural anesthesia and general anesthesia for laparoscopic cholecystectomy, patients in the surgery and the effectiveness of anesthesia after surgery, the incidence of side effects or complications, and postoperative recovery of the body of the differences

Condition
Epidural Anesthesia Laparoscopic Cholecystectomy

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Comparison Epidural Anesthesia and General Anesthesia in Laparoscopic Cholecystectomy

Resource links provided by NLM:


Further study details as provided by National Taiwan University Hospital:

Estimated Enrollment: 100
Study Start Date: April 2011
Estimated Study Completion Date: April 2014
Estimated Primary Completion Date: June 2013 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   20 Years to 70 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Underwent laparoscopic cholecystectomy in patients
Criteria

Inclusion Criteria:

  • Underwent laparoscopic cholecystectomy in patients

Exclusion Criteria:

  • Unconsciousness or can not express their own feelings of the patient
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01398683


Sponsors and Collaborators
National Taiwan University Hospital
Investigators
Principal Investigator: Yao Ming Wu, Bachelor National Taiwan University Hospital
  More Information

Responsible Party: National Taiwan University Hospital
ClinicalTrials.gov Identifier: NCT01398683     History of Changes
Other Study ID Numbers: 201104080RC
First Submitted: July 19, 2011
First Posted: July 20, 2011
Last Update Posted: November 16, 2012
Last Verified: July 2011

Additional relevant MeSH terms:
Anesthetics
Central Nervous System Depressants
Physiological Effects of Drugs