Post operative analgesic effect of intra-articular ropivacaine at the start and end of hip arthroscopy

Not Applicable

Completed

• Conditions: femoro-acetabular impingement; labral tear; postoperative pain; Musculoskeletal - Other muscular and skeletal disorders; Anaesthesiology - Pain management

• Registration Number: ACTRN12614001121651
• Lead Sponsor: Dr Phong Tran

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-10-23
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 132

Inclusion Criteria

All adult patients attending hip arthroscopy at Bellbird Private Hospital performed by the senior author will be eligible to participate in the study.

Exclusion Criteria

Patients will be excluded from the study if they had previous hip surgery, aged less than 18 or more than 75 years, diagnosis of chronic pain syndrome, contraindications to or allergic reactions to any of the standardized analgesic/ anaesthesia medication or local infiltrate components, ASA 3 or more and those requiring ketamine analgesia or regional block.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain: measured by - 1) Postoperative VAS (Visual Analogue Scale) after 0.5, 1, 2, 4, 8, 12, and 2) 24 hours, highest and lowest recovery room NRS (numerical rating scale)[Pain measured at: 1) Recovery time and the following time points of: 2)<br>0.5,1,2,4,8,12 and 24 hrs postoperative]

Secondary Outcome Measures

Name	Time	Method
Recovery room morphine requirements - prospective recording of mg and mg/kg intravenous morphine administered until pain score < or = 6/10<br>[recovery room time<br>24 hourly postoperative ward];Recovery room antiemetic requirements - prospective recording of mg of ondansetron and/ or cyclizine administered until cessation of vomiting [Duration of stay in recovery room];24 hourly ward analgesia requirements - prospective recording of mg and mg/kg subcutaneous morphine and/ or oral oxycodone required for patient satisfaction or pain score < or =6/10[time from discharge to ward until 24 hours from start of surgery];24 hourly ward antiemetic requirements - prospective recording of mg of ondansetron and/ or cyclizine administered until cessation of vomiting <br><br>[time from discharge to ward until 24 hours from start of surgery];Median Recovery room NRS-11 score[Duration of stay in the recovery room]