Try our beta test site
IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more...

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
Information provided by (Responsible Party):
National Taiwan University Hospital Identifier:
First received: July 19, 2011
Last updated: November 15, 2012
Last verified: July 2011
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

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)

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

Inclusion Criteria:

  • Underwent laparoscopic cholecystectomy in patients

Exclusion Criteria:

  • Unconsciousness or can not express their own feelings of the patient
  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 identifier: NCT01398683

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

Responsible Party: National Taiwan University Hospital Identifier: NCT01398683     History of Changes
Other Study ID Numbers: 201104080RC
Study First Received: July 19, 2011
Last Updated: November 15, 2012

Additional relevant MeSH terms:
Central Nervous System Depressants
Physiological Effects of Drugs processed this record on May 24, 2017