Postoperative evaluation using different tourniquet cuff pressure in simultaneous bilateral total knee arthroplasty a double-blind randomised controlled trial~

Postoperative evaluation using different tourniquet cuff pressure in simultaneous bilateral total knee arthroplasty a double-blind randomised controlled trial~ - Postoperative evaluation using different tourniquet cuff pressure in simultaneous bilateral total knee arthroplasty

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000029287

Enrollment

Registered

2017-10-01

Start date

2017-10-01

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

Osteoarthritis of knee

Interventions

The tourniquet cuff pressure was decided by measuring the limb occlusion pressure. The conventional tourniquet cuff pressure was 300mmHg.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients scheduled for simultaneous bilateral primary total knee arthroplasty.

Exclusion criteria

Exclusion criteria: A patient who can not use tourniquet,who changed the tourniquet cuff pressure during surgery,and who judged that doctor is ineligible.

Design outcomes

Primary

Measure	Time frame
Changes in thigh pain from preoperative to 24 hours postoperatively.	—

Countries

Japan

Contacts

Public ContactKenka Ra

Naniwa Ikuno Hospital Joint Reconstruction Center

l_c_h_4160@yahoo.co.jp06-6632-9915

Outcome results

None listed

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