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Clinical Trials/NCT04547595
NCT04547595
Recruiting
Phase 3

Assessment of Efficacy of Hypnosis Intervention During Lavage Procedure for Knee Osteoarthrosis

Assistance Publique - Hôpitaux de Paris1 site in 1 country100 target enrollmentOctober 6, 2021

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
100
Locations
1
Primary Endpoint
Pain assessed by Visual Analog Scale
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to determine whether hypnosis intervention added to usual care is more effective than usual care alone to control pain during lavage procedure in patients with knee osteoarthrosis

Detailed Description

Joint lavage can be used in acute knee osteoarthritis, and can be repeated when it is effective. This procedure can generate pain and anxiety which are prevented by systematic prescription of analgesics and anxiolytics. To assess the benefit of hypnosis intervention, the investigators designed a monocentric prospective controlled randomised, single-blind study. Patients with acute and painful knee osteoarthritis, having an indication of lavage according to the rheumatologist, will be randomized to standard care, versus standard care and hypnosis. The hypothesis is that hypnosis intervention will decrease the level of pain during lavage, and the analgesics consumption during the week following the lavage. The sample size will be 100, 50 patients per group. Inclusion is scheduled for 18 months, and duration of the study will be 2 years. The main efficacy criterion is the pain score (assessed using VAS) difference between the 2groups; no interim analysis will be performed.

Registry
clinicaltrials.gov
Start Date
October 6, 2021
End Date
April 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • diagnosis of knee osteoarthritis
  • indication for a lavage

Exclusion Criteria

  • People who have had both knees washed on the same day.
  • People who have already received a joint lavage.
  • Patients with psychotic disorders.
  • Refusal to participate.
  • People who do not understand and/or speak French or who are deaf.

Outcomes

Primary Outcomes

Pain assessed by Visual Analog Scale

Time Frame: One Day, at end of lavage procedure

VAS range 0-10, 10 for most severe pain

Secondary Outcomes

  • Operator Impact(Over 1 week after lavage procedure)
  • Anxiety assessed by Visual Analog Scale(Day 1, at end of lavage procedure)
  • Pain assessed by Visual Analog Scale(Day 7, after lavage procedure)
  • Gesture tolerability(Day 1, at end of lavage procedure)
  • Analgesics consumption(Over 1 week after lavage procedure)

Study Sites (1)

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