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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 13 April 2015
Main ID:  NCT02244177
Date of registration: 10/09/2014
Prospective Registration: No
Primary sponsor: Kaohsiung Veterans General Hospital.
Public title: Relationship of Essential Hypertension and Its Treatments on the Postoperative Pain Management: a Prospective, Observational, Cross-sectional Study
Scientific title:
Date of first enrolment: November 2013
Target sample size: 300
Recruitment status: Recruiting
URL:  http://clinicaltrials.gov/show/NCT02244177
Study type:  Observational
Study design:  Observational Model: Cohort, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
Taiwan
Contacts
Name:     Yuan Yi Chia, Bachelor
Address: 
Telephone: 88673468183
Email: yychia@isca.vghks.gov.tw
Affiliation: 
Name:     Yuan Yi Chia, Bachelor
Address: 
Telephone: 88673468183
Email: yychia@isca.vghks.gov.tw
Affiliation: 
Key inclusion & exclusion criteria

Inclusion Criteria:

- 300 eligible subjects

- No contraindication for inhalation anesthesia

- Elective surgery

- Age between 20-75 y/o

- No contraindication for postoperative morphine pain control

- Female or male

- Essential hypertension stage I and II (140<=SBP<=180; 90<=DBP<=110)

Exclusion Criteria:

- Liver disease

- Renal disease

- Those who is presumed to go to ICU after surgery

- The patients with dementia or conscious disturbance

- Pregnancy or breast feeding

- Secondary hypertension

- events in recent 6 months myocardial infarction cardiac bypass surgery unstable
angina cerebrovascular events congestive heart failure significant arrhythmia
thoracic surgery



Age minimum: 20 Years
Age maximum: 75 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Hypertension
Intervention(s)
Primary Outcome(s)
Pain [Time Frame: Post-operation Day1 to Day4]
Secondary Outcome(s)
Morphine consumption [Time Frame: Post-operation Day1 to Day4]
Secondary ID(s)
VGHKS-103-080
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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