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NCT03789266 Clinical Trial

Drains Ablation Post Total Hip Arthroplasty : Search for the Least Painful Technique

Total Hip Arthroplasty Clinical Trial

— TADDA  

Official title:
Drains Ablation Post Total Hip Arthroplasty : Search for the Least Painful Technique

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03789266
Other study ID # 2016/382/HP
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 19, 2018
Est. completion date June 2020

Study information
Verified date June 2020
Source University Hospital, Rouen
Contact Mylène BONNAIRE, Ms
Phone +3323288
Email mylene.bonnaire@chu-rouen.Fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of ablation technique of drains

Recruitment information / eligibility
Status Recruiting
Enrollment 116
Est. completion date June 2020
Est. primary completion date June 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Patients admitted to the orthopedic surgery department for surgery for a total hip arthroplasty

2. Signed inform consent form

Exclusion Criteria:

1. Drain in non-aspirating mode at the time of medical ablation prescription

2. Administration of analgesic III in the 12 hours preceding the inclusion

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• drain ablation
drain ablation will be done in Aspiration mode or in non Aspiration mode

Locations
Country Name City State
France Rouen University Hospital Rouen

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Rouen

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Evaluate the pain felt by the patients at the time of the removal of the drain, using the pain visual analogue scale pain will be measured using a visual analogic scale from 0 (for no pain) to 10 (fo maximum pain) 20 minutes
Secondary Presence of haematoma after ablation Presence or absence of haematoma will be visually checked Day 2 post ablation
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