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Exploratory clinical trial on intraoperative intestinal blood flow assessment using ultrasound doppler technique

Exploratory clinical trial on intraoperative intestinal blood flow assessment using ultrasound doppler technique

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs032240428
Enrollment
8
Registered
2024-10-23
Start date
2024-10-23
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

colorectal cancer colorectal cancer

Interventions

Evaluation of blood flow in the intestinal wall using ultrasound doppler technique before anastomosis during colorectal cancer surgery.
ultrasound, dopler, ICG

Sponsors

Hirata Atsushi
Lead Sponsor
Matsubara Hisahiro
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who are histologically proven to be col orectal cancer 2) Patients undergoing colorectal cancer surgery with gastrointestinal anastomosis 3) Patients whose age at registration is 20 years or older 4) Patients with General State Performance Status (ECOG) 0 to 2 5) Patients whose functions of the main organs are adequately maintained and judged to be safe for surgery by the doctor incharge of examination 6) Patients who have received sufficient explanations about participation in this study and have giv en written consent of their own free will with sufficient understanding.

Exclusion criteria

Exclusion criteria: 1) Patients with a history of allergy to ICG or iodine hypersensitivity 2) Pregnant, possibly pregnant, within 28 days pos tpartum, breastfeeding 3) Other patients judged inappropriate by the exa mining physicia

Design outcomes

Primary

MeasureTime frame
Difference in blood flow boundary between ultrasound doppler method and ICG method

Secondary

MeasureTime frame
Reproducibility of ultrasound doppler method Incidence of intraoperative adverse events Adverse events within 30 days after surgery Postoperative hospital stay

Contacts

Public ContactAtsushi Hirata

Chiba University Hospital

a.hirata@chiba-u.jp+81-43-222-7171

Outcome results

None listed

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