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A comparative analysis of IPP test and traditional method on the diagnosis of sacroiliac joint dysfunction

Research on Key Technologies of intelligent limb function rehabilitation evaluation and assistive device adaptation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048513
Enrollment
Unknown
Registered
2021-07-09
Start date
2019-01-25
Completion date
Unknown
Last updated
2022-03-21

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

Conditions

sacroiliac joint dysfunction

Interventions

Gold Standard:Convenience method: the Sacroiliac joint dysfunction diagnosis was confirmed by sacroiliac joint injection, with relief of low back pain and leg discomfort more than 75%
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Sponsors

China Rehabilitation Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Criteria of CSIJD group: male or female between age 20–60 years; The main complaint of the patients was pain in the posterior sacroiliac joint with or without leg discomfort. MRI of the lumbar spine showed no or mild LDH. The CSIJD diagnosis was confirmed by sacroiliac joint injection, with relief of low back pain and leg discomfort more than 75%. Criteria of LDH group: male or female between age 20–60; low back pain with radiation to the lower extremities for more than 6 months; and lumbar MRI with lumbar disc herniation or disc prolapse. The diagnosis of LDH was confirmed according to the 2014 North American Spine Association diagnosis and treatment guidelines for LDH, and the symptoms and signs were consistent with the herniated segment on MRI. Criteria of control (healthy) group: male or female between age 20–60 years; without any pain of low back, leg or pelvic region within 1 year.

Exclusion criteria

Exclusion criteria: fracture, infection, tumor and operation history of pelvic, hip joint, lumbar spine;hip degeneration;lumbar spinal stenosis, lumbar spondylolisthesis and lumbar scoliosis, and others who can not cooperate with physical examination.;

Design outcomes

Primary

MeasureTime frame
IPP tests;tradition provocation tests;

Countries

China

Contacts

Public ContactBai Jinzhu

China Rehabilitation Research Center

baijinzhu@126.com+86 13681240899

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026