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NCT01095536 Clinical Trial

Risk Factors for Shoulder Pain and Emesis After Laparoscopic Cholecystectomy

Shoulder Pain Clinical Trial

Official title:
The Observational Cohort Study to Identify Risk Factors for Shoulder Pain and Emesis After Laparoscopic Cholecystectomy Under General Anesthesia

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01095536
Other study ID # 201001019IC
Secondary ID
Status Recruiting
Phase N/A
First received March 28, 2010
Last updated October 4, 2010
Start date February 2010
Est. completion date February 2011

Study information
Verified date March 2010
Source Taipei Veterans General Hospital, Taiwan
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial Summary

Risk factors for postoperative shoulder pain after laparoscopic cholecystectomy were not clear. Moreover, risk factors for postoperative emesis specially for this surgery were not detailed and accurate. The present study is a prospective cohort study to identify risk factors for shoulder pain and emesis within 24 hours in Chinese patients after laparoscopic cholecystectomy under general anesthesia.

Description:

The present study is a prospective cohort study to identify risk factors for shoulder pain and emesis within 24 hours in Chinese patients after laparoscopic cholecystectomy under general anesthesia.

Recruitment information / eligibility
Status Recruiting
Enrollment 380
Est. completion date February 2011
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender Both
Age group 21 Years and older
Eligibility Inclusion Criteria:

- > 21 years old,

- Chinese patient

Exclusion Criteria:

- current pregnancy,

- patients with history of upper laparotomy,

- inability to communicate before operation,

- persistent emesis or shoulder pain before operation,

- patients who converted to open cholecystectomy,

- receiving postoperative ventilator support,

- unstable postoperative condition or major complications.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Taiwan Department of Anesthesiology, Taipei Veterans General Hospital Taipei

Sponsors (1)
Lead Sponsor Collaborator
Taipei Veterans General Hospital, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary incidence of postoperative shoulder pain and emesis within postoperative 24 hours No
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