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Clinical Trials/EUCTR2006-003737-33-SE
EUCTR2006-003737-33-SE
Active, not recruiting
Not Applicable

Continuous Intraperitoneal Infusion of Local Anesthetics vs. Patient Controlled Intraperitoneal injection for Postoperative Pain relief following Abdominal Hysterectomy. A randomized, double-blind study

Örebro University Hospital0 sitesSeptember 7, 2006
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ConditionsPostoperative pain after open abdominal hysterectomy
DrugsChirocaine

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative pain after open abdominal hysterectomy
Sponsor
Örebro University Hospital
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 7, 2006
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
Örebro University Hospital

Eligibility Criteria

Inclusion Criteria

  • •18 –65 year old patients undergoing open abdominal hysterectomy.
  • •Have signed and dated Informed Consent.
  • •Willing and able to comply with the protocol for the duration of the trial.
  • •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
  • •F.1\.3 Elderly (\>\=65 years) no
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •Patients undergoing open abdominal hysterectomy due to suspected cancer.
  • •Patients with chronic pain who are taking analgesics regularly.
  • •Allergy to components in levobupivacaine (Chirocaine)/Saline (Sodium Chloride).
  • •Participation in other clinical trials.

Outcomes

Primary Outcomes

Not specified

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