Spinal manipulation in the treatment of patients with lumbar disc herniation who had sacroiliac joint hypomobility

Spinal manipulation in the treatment of patients with MRI-confirmed lumbar disc herniation who had sacroiliac joint hypomobility: a quasi-experimental study

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017011924149N33

Enrollment

Registered

2017-02-19

Start date

2009-09-23

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

lumbar disc herniation. Other specified intervertebral disc displacement

Interventions

Intervention: five sessions of lumbar rotational and sacroiliac joint manipulation, every other day.

Treatment - Other

Intervention: five sessions of lumbar rotational and sacroiliac joint manipulation, every other day

Eligibility

Sex/Gender

All

Age

20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age between 20 and 50 years old; MRI-proven unilateral lumbar disc herniation; Symptomatic lumbar disc disease at one segment( L4-L5 or L5-S1); Ipsilateral sacroiliac joint hypomobility; Leg pain during one to 10 months before the study; Leg pain over previous 24 hours should be 30-70 out of 100 Exclusion criteria: Sequestrated lumbar disc herniation; Spinal canal stenosis; Spondylolysthesis; Previous lumbar surgery; Gross instability; Positive SLR test

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain intensity. Timepoint: Before, Immediately, 3rd session, 5th session and a month after intervention. Method of measurement: VAS.;Disability level. Timepoint: Before, 3rd session, 5th session and a month after intervention. Method of measurement: Oswestry pain and disability questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFahimeh Kamali

School of Rehabilitation Sciences, Shiraz University of Medical Sciences

kamalif@sums.ac.ir+98 71 3627 1551

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 6, 2026