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Clinical Trials/NCT01747005
NCT01747005
Unknown
Not Applicable

Effect of Enhanced Recovery After Surgery (ERAS) on Inflammatory Response After Planned Abdominal Hysterectomy: A Prospective Randomized Clinical Trial.

Antypin Eduard Eduardovich1 site in 1 country80 target enrollmentJune 2012
ConditionsHysterectomy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hysterectomy
Sponsor
Antypin Eduard Eduardovich
Enrollment
80
Locations
1
Primary Endpoint
Change of Serum level of IL-1beta,IL-6,CRP,Cortisol,IL-4 by immuno-ferment analysis.
Last Updated
10 years ago

Overview

Brief Summary

The aim of study is to determine effect of enhanced recovery after surgery (ERAS) on inflammatory response after abdominal hysterectomy.

Registry
clinicaltrials.gov
Start Date
June 2012
End Date
December 2015
Last Updated
10 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Antypin Eduard Eduardovich
Responsible Party
Sponsor Investigator
Principal Investigator

Antypin Eduard Eduardovich

Anesthesiologist

Samoilova Maternity Home

Eligibility Criteria

Inclusion Criteria

  • Informed consent
  • Abdominal hysterectomy
  • ASA class I or II

Exclusion Criteria

  • psychiatric disorders
  • ASA III and IV
  • Chronic inflammatory disorders
  • Pregnancy
  • Local anesthetics allergy
  • Coagulation disorders
  • patients receiving anticoagulants

Outcomes

Primary Outcomes

Change of Serum level of IL-1beta,IL-6,CRP,Cortisol,IL-4 by immuno-ferment analysis.

Time Frame: baseline, 24 hour post-operative and 7 days post-operative

Secondary Outcomes

  • Change of postoperative pain, fatigue and postoperative nausea and vomiting(baseline,6,12,24,48 hour and 7 days postoperatively)

Study Sites (1)

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