NCT02771041

Brief Summary

Arthroplastic hip surgery "fast-track" the subject of increasing interest and reduces the average length of stay and improve patient satisfaction. This fast circuit implemented in many schools uses dedicated inpatient units, preoperative patient education in multidisciplinary groups (including physiotherapists, nurses, rehabilitation doctors and surgeons), an analgesia protocol multimodal and a network dedicated to the outlet (1.2). The investigators working hypothesis is that the mere realization of a preoperative visit a week before the intervention would reduce the average length of stay for all patients with a target of two nights (instead of 7.5 days currently) (3) to reduce the use of SSR during hospitalization. This consultation would serve to explain to the patient the early course of care, give advice and help to anticipate acts for its release "post-operative" as, for example, contact a physical therapist and a nurse or check to their community pharmacy if their heparin stock is enough and to answer any questions (Appendix 2: early information given to the patient consultation J-8). The investigators protocol is inspired by the one already in place for outpatient PTH and PTH 1 night but invariably apply to all patients for whom a home is considered output.

Trial Health

15
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Sep 2015

Shorter than P25 for not_applicable

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 23, 2015

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2016

Completed
8 days until next milestone

First Submitted

Initial submission to the registry

May 9, 2016

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 12, 2016

Completed
Last Updated

February 23, 2017

Status Verified

May 1, 2016

Enrollment Period

7 months

First QC Date

May 9, 2016

Last Update Submit

February 21, 2017

Conditions

Keywords

Hip prothesis

Outcome Measures

Primary Outcomes (1)

  • Average length of stay

    After surgery at Day 1

Secondary Outcomes (6)

  • OXFORD Score for Hip

    Before and after surgery at Day -1 then Day 1

  • Patient satisfaction (verbal scale: 0 to 10)

    Before and after surgery at Day -1 then Day 1

  • St. Joseph Satisfaction

    After surgery when leaving the hospital, in average in the 3 Days

  • Evaluation of pain by VAS

    Before and after surgery at Day -1 then Day 1

  • Morbidity

    In the week after surgery

  • +1 more secondary outcomes

Study Arms (2)

Group with D-8 medical consultation

EXPERIMENTAL

A medical consultation 8 days before surgery would serve to explain to the patient the early course of care, give advice and help to anticipate acts for its release "post-operative" as, for example, contact a physical therapist and a nurse or check to their community pharmacy if their heparin stock is enough and to answer any questions.

Procedure: medical consultation 8 days before surgery

Group without D-8 medical consultation

NO INTERVENTION

Interventions

This consultation would serve to explain to the patient the early course of care, give advice and help to anticipate acts for its release "post-operative" as, for example, contact a physical therapist and a nurse or check to their community pharmacy if their heparin stock is enough and to answer any questions.

Group with D-8 medical consultation

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \. All patients undergoing total hip replacement

You may not qualify if:

  • Patient choosing immediately a supported SSR in postoperative
  • Geographical remoteness
  • Social isolation
  • Medical pathology requiring special monitoring (phlebitis history, coagulation disorders, anticoagulant therapy ...)
  • psychiatric pathology
  • Patients opting for the protocol "overnight"

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Guillaume RIOUALLON, MD

    Groupe Hospitalier Paris Saint-Joseph (FRANCE)

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 9, 2016

First Posted

May 12, 2016

Study Start

September 23, 2015

Primary Completion

May 1, 2016

Study Completion

May 1, 2016

Last Updated

February 23, 2017

Record last verified: 2016-05