The clinical efficacy of lordotic curve controlled traction device

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004934

Enrollment

Registered

2020-04-16

Start date

2020-05-04

Completion date

Unknown

Last updated

2020-04-21

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

Conditions

None listed

Interventions

Medical Device : A total of 90patients with intervertebral disc disease were recruited and randomly assigned to either the RLCCT(Lordotic Curve Controlled Traction with Rotational Technique), LCCT(lor

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patient with cervical, lumbar intervertebral disc disease at the C5/6, L4/5 or L5/S1 level as confirmed by MRI

Exclusion criteria

Exclusion criteria: tumor, pregnant, Patients with rheumatoid arthritis, traumatic brain injury and stroke, glaucoma, unstable vertebrae or previous history of operation on spine

Design outcomes

Primary

Measure	Time frame
X-ray	—

Secondary

Measure	Time frame
neck disability index (NDI), patient-specific functional scale (PSFS), Visual Analogue Scale(VAS), oswestry disability index (ODI), The Roland-Morris Low Back Pain and Disability(RM)	—

Countries

Korea, Republic of

Contacts

Public ContactChang Lee

Pusan National University Yangsan Hospital

Outcome results