Prosthetic suspension system

Design, development and clinical evaluation of a new prosthetic suspension system for lower limb amputees

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013061813706N1

Enrollment

Registered

2013-07-02

Start date

2012-03-21

Completion date

Unknown

Last updated

2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower limb amputation.

Interventions

New prosthetic suspension system, Pin/lock system, Seal-In system.

Treatment - Devices

New prosthetic suspension system, Pin/lock system, Seal-In system

Eligibility

Sex/Gender

All

Age

20 Years to 80 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria would be: - lower limb amputee - age 20 to 80 - no medical contraindications for engaging in physical activities - no ulcer or open wound in the limb - old prosthetic user (more than 1 month) - no upper limb weakness or disability Exclusion criteria: - ulcer or open wound in the limb - Serious health condition (heart attack, dialysis, ...)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Ambulation. Timepoint: 4 weeks after use. Method of measurement: kinematic & kinetic gait analysis.	—

Secondary

Measure	Time frame
Interface pressure. Timepoint: 4 weeks after use. Method of measurement: Pressure mapping.	—

Countries

Malaysia

Contacts

Public ContactNoor Azuan Abu Osman

University of Malaya

azuan@um.edu.my006379675201

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 8, 2026