Skip to main content
Clinical Trials/EUCTR2010-024538-51-ES
EUCTR2010-024538-51-ES
Active, not recruiting
Not Applicable

Study of the effects of pregabalin in postoperative pain control in general total intravenous anesthesia, general inhalation anesthesia and combined anesthesiaafter abdominal hysterectomy. - Pregpost

Silvia Gil Trujillo0 sitesJanuary 19, 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
The presence of acute postoperative pain remains a major cause of preoperative morbidity.The objective is to evaluate the analgesic efficacy of pregabalin in thepostoperatory of abdominal hysterectomy associated with 3 types of anesthesia.
Sponsor
Silvia Gil Trujillo
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 19, 2012
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
Silvia Gil Trujillo

Eligibility Criteria

Inclusion Criteria

  • Patients scheduled for abdominal hysterectomy. \-Age 18\-70 years. \- ASA I\-II
  • (anesthetic classification system to estimate the risk posed by anesthesia for the different states of the patient, I: no associated pathology and II: mild systemic
  • disease, uncontrolled and disabling)\-no known allergies to drugs to manage in the study. \- Laboratory tests in the range of normal, and negative pregnant test.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 100
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 80

Exclusion Criteria

  • Impaired renal function. \- History of alcohol or drugs. \- Treatment with antacids and antidepressants. \- History of diabetes or epilepsy. \- Chronic treatment with steroids or at least 4 weeks before surgery. \- Mental illness or inability to understand the Spanish. Pregnant women.

Outcomes

Primary Outcomes

Not specified

Similar Trials