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Trial to monitor percutaneous oxygen saturation in autologous tissue transplantation

Trial to monitor percutaneous oxygen saturation in autologous tissue transplantation - Trial to monitor percutaneous oxygen saturation in autologous tissue transplantation

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000025197
Enrollment
50
Registered
2016-12-09
Start date
2011-01-01
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

Autologous tissue transplantation

Interventions

A solution of 25 mg of indocyanine green in 10 ml of injection solution was intravenously administered 2 ml of indocyanine green solution per angiogram.

Sponsors

Kouchi medical school
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: A case of reconstructive surgery performed with free tissue transplant with a vascular pattern (muscle flap or jejunal graft) in the Department of Plastic Surgery, Kochi University School of Medicine affiliated hospital for 6 years from 1 January 2011 to 31 December 2017.

Exclusion criteria

Exclusion criteria: Rebuilding surgery in the oral cavity and cases where the neck is short and the sensor can not be affixed after the jejunal transplantation do not undergo continuous surgical monitoring after surgery.

Design outcomes

Primary

MeasureTime frame
Trend of changes in intraoperative and postoperative blood flow dynamics and tissue oxygen saturation.—

Countries

Japan

Contacts

Public ContactSuzumi Oono

Kouchi medical school Surgery (Surgery 2)

im32@kochi-u.ac.jp0888802375

Outcome results

None listed

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