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A randomized phase II study to evaluate efficacy of negative pressure wound therapy on prophylaxis of the incisional hernia after reversal of temporaly diverting stoma

Phase 2
Recruiting
Conditions
temporally diverting stoma to be planned to have closed
Registration Number
JPRN-UMIN000030936
Lead Sponsor
Aichi Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria

Not provided

Exclusion Criteria

severe skin disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
rate of incidence of radiological incisional hernia after one year of surgery
Secondary Outcome Measures
NameTimeMethod
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