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Sub Analysis for cohort study 'perioperative impact for ADL' with patients admitted to Intensive Care unit

Not Applicable
Conditions
All patients recieving medical care in perioperative center in our hospital
Registration Number
JPRN-UMIN000021705
Lead Sponsor
ara Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
3000
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who is not able to answer quetionnaire in Japanese Patients requiring reoperation

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
SF-8, TMIG, WHODAS 2.0
Secondary Outcome Measures
NameTimeMethod
variables that affect primary outcomes
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