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Comparison Epidural Anesthesia and General Anesthesia in Laparoscopic Cholecystectomy

This study is enrolling participants by invitation only.
Sponsor:
Information provided by (Responsible Party):
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT01398683
First received: July 19, 2011
Last updated: November 15, 2012
Last verified: July 2011
  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

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

Ages Eligible for Study:   20 Years to 70 Years
Genders Eligible for Study:   Both
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
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: NCT01398683

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

No publications provided

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

Additional relevant MeSH terms:
Anesthetics
Central Nervous System Agents
Central Nervous System Depressants
Pharmacologic Actions
Physiological Effects of Drugs
Therapeutic Uses

ClinicalTrials.gov processed this record on November 20, 2014