Skip to main content
Clinical Trials/ACTRN12614000371695
ACTRN12614000371695Completed未知

Segmental Epidural Anaesthesia and Its Effect on Postoperative Analgesic Requirement in Adult Patients Undergoing Elective Percutaneous Kyphoplasty Operation.

Alparslan APA0 sites44 target enrollmentStarted: April 8, 2014Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
44

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomised controlled trial
Primary Purpose
Treatment
Masking
Blinded (masking used)

Eligibility Criteria

Ages
18 Years to 85 Years (—)
Sex
All

Inclusion Criteria

  • Fifty two ASA class I to III patients aged over 18 years scheduled for percutaneous kyphoplasty were recruited to the study.

Exclusion Criteria

  • Severe systemic disease includes ASA class IV and more, pathology in cervical vertebra, known allergy to the study drugs, any contraindication for performing the epidural anaesthesia (bleeding diathesis, anticoagulation, hypovolemia, infection at the site of injection, increased intracranial pressure, severe aortic stenosis, severe mitral stenosis), presence of pregnancy, and cognitive disorders that preventing the cooperation were accepted as exclusion criteria. Patients requiring more than one level of intervention were excluded, also.

Investigators

Sponsor
Alparslan APA

Similar Trials