Multicenter, single-group, postoperative, clinical evaluation of patient treated with Sugita-clip.

Multicenter, single-group, postoperative, clinical evaluation of patient treated with Sugita-clip. - Multicenter, single-group, postoperative, clinical evaluation of patient treated with Sugita-clip.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000036813

Enrollment

400

Registered

2019-07-01

Start date

2019-07-01

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

cerebral aneurysm

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) Patients who underwent clipping surgery for ruptured or unruptured cerebral aneurysms using the device from 1 January 2016 to 31 December 2017 (during the past 2 years). (2) Patients who are evaluated by using mRS (3) Patients who are at least 20 years old at the time of surgery (cerebral aneurysm clipping).

Exclusion criteria

Exclusion criteria: Patients who have indicated their intention (opt-out) to refuse to participate in this study

Design outcomes

Primary

Measure	Time frame
To evaluate the progress of patients treated with the device by using the postoperative Modified Rankin Scale(mRS).	—

Countries

Japan

Contacts

Public ContactKenji Uda

Nagoya University School of Medicine Hospital Department of Neurosurgery

kenji84u@med.nagoya-u.ac.jp052-744-2353

Outcome results