ACTRN12614001161617Completed未知
The effect of intraperitoneal Ropivacaine on post-laparoscopic pain in appendicectomy patients compared with the effect of intraperitoneal normal saline.
Armadale and Kelmscott Memorial Hospital0 sites86 target enrollmentStarted: November 4, 2014Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 86
Study Overview
Brief Summary
A total of 86 patients were included in the study. During the immediate post-operative period from 0-6 hours, there was a reduction in the number of times the patient control pain drug release button was pressed in the local anaesthetic ropivacaine group compared to the normal saline group. This suggest intraperitoneal use of local anaesthetic is a useful adjunct for post operative pain management.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Treatment
- Masking
- Blinded (masking used)
Eligibility Criteria
- Ages
- 18 Years to 80 Years (—)
- Sex
- All
Inclusion Criteria
- •All patients undergoing laparoscopic appendicectomy at Armadale Hospital
Exclusion Criteria
- •1. Medical or psychiatric conditions that compromise patient’s ability to give informed consent
- •2. Pregnant or breast feeding
- •3. Allergies to paracetamol, fentanyl or ropivacaine.
- •4. Liver failure
- •5. Conversion from laparoscopic surgery to open surgery
- •6. Presence of faecal peritonitis
- •7. ASA III
- •8. Iatrogenic perforation
- •9. Chronic pain syndrome
- •10. Operative time more than 2 hours.
- •11. Drain insertion
- •12. Weight >100kg
Investigators
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