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

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 - Negative pressure wound therapy on the prophylaxis of the incisional hernia

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000030936

Enrollment

Registered

2018-01-22

Start date

2018-01-22

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

temporally diverting stoma to be planned to have closed

Interventions

Negative Pressure Wound Therapy for seven to eight days standard stoma reversal

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with temporally stoma to be planned to have closed who had received initial surgery at our institution

Exclusion criteria

Exclusion criteria: severe skin disease

Design outcomes

Primary

Measure	Time frame
rate of incidence of radiological incisional hernia after one year of surgery	—

Countries

Japan

Contacts

Public ContactTatsuki Matsumura

Aichi Medical University Gastroenterological Surgery

matsumura.tatsuki.739@mail.aichi-med-u.ac.jp0561-62-3311

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026