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Safety and Efficacy of Radiotherapy Combined with a Nonwoven Fabric Bioabsorbable Spacer

Safety and Efficacy of High Precision Radiotherapy Combined with a Nonwoven Fabric Bioabsorbable Spacer for Tumors Located Colse to Gastrointestinal Tract : Space Making Radiotherapy - SMRT

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs052220157
Enrollment
9
Registered
2023-01-24
Start date
2023-09-06
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

pancreatic cancer, biliary tract cancer, kideny cancer, etc. gastrointestinal proximal malignant tumors

Interventions

Placement of an absorbable spacer between the gastrointestinal tract and the tumor to secure a safer distance for curative radiotherapy for gastrointestinal proximal malignant tumors
D013511
absorbable spacer placement

Sponsors

Sasaki Ryohei
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Those who have abdominal or pelvic tumors pathologically diagnosed as malignant. 2) Those who are indicated for high-dose radiotherapy such as Intensity Modulated Radiation Therapy (IMRT) or Stereotactic Body Radiation Therapy (SBRT). 3) Those who have located tumor within a certain radiation field. 4) Those who have narrow gap between malignant tumor and surrounding organs (10mm or less). 5) Those who are judged to be able to place a spacer and receive radiotherapy according to the protocol. 6) Those who have an Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0-2 at the time of informed consent. 7) The function of major organs is preserved. 8) Those who are 20 years of age or older at the time of obtaining consent. 9) Those who can fill out the consent form about participation in this clinical research by themselves.

Exclusion criteria

Exclusion criteria: 1) Expected prognosis is less than 6 months. 2) Those who have a history of radiation therapy at the treatment area in this study.. 3) Those who have an active gastrointestinal ulcer. 4) Those who have an ascites or pleural effusion suspected to be malignant. 5) Those who have a metal stent placed near the irradiation field. 6) Those who cannot use iodine contrast media or gadolinium contrast media. 7) Those who are allergic to polyglycolic acid. 8) Those who have an active infection at the treatment area. 9) Those who are judged to be inappropriate by the person in charge of this research.

Design outcomes

Primary

MeasureTime frame
PTV V95(%) before and after absorbable spacer placement

Secondary

MeasureTime frame
Efficacy endpoint 1) Dose distribution 2) Completion of radiotherapy Safety endpoint 1) Occurrence of diseases 2) Defects and their details in absorbable spacer

Contacts

Public ContactSatoshi Seno

Kobe University Hospital

ano.senoodesuga@gmail.com+81-78-382-5687

Outcome results

None listed

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