The effect of soft tissue release of the thoracic on the improvement of pain, in patients with failed back surgery syndrome

The effect of soft tissue release of the thoracic on the improvement of pain, disability, and quality of life in patients with failed back surgery syndrome

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230212057390N3

Enrollment

Registered

2023-10-12

Start date

2023-10-23

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

failed back surgery syndrome. ???? ?? ????? ??????? ???

Interventions

Intervention 1: Intervention group: The patient is lying on the stomach and the hands are turned inward and attached to the patient s trunk, then the therapist is placed near the patient and places th

Eligibility

Sex/Gender

All

Age

20 Years to No maximum

Inclusion criteria

Inclusion criteria: failed back surgery Not using drugs affecting the functioning of the automatic nervous system

Exclusion criteria

Exclusion criteria: 1. Patients with a history of spinal fracture 2. Patients with spine abnormalities 3. Patients with fear of light 4. Patients with dysfunctional autonomic nervous system 5. Patients with skin sensitivity 6. Patients with alcohol addiction 7. Patients with Horner's syndrome

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: At the start of the trial, five days later, ten days later, and one month afterwards. Method of measurement: Visual analog scale of pain.;Disability. Timepoint: At the start of the trial, five days later, ten days later, and one month afterwards. Method of measurement: Oswestry Disability Index.;Quality of Life. Timepoint: At the start of the trial, five days later, ten days later, and one month afterwards. Method of measurement: Functional rating index.;Blood pressure. Timepoint: At the start of the trial, five days later, ten days later, and one month afterwards. Method of measurement: Sphygmomanometer.	—

Measure

Time frame

Pain. Timepoint: At the start of the trial, five days later, ten days later, and one month afterwards. Method of measurement: Visual analog scale of pain.;Disability. Timepoint: At the start of the trial, five days later, ten days later, and one month afterwards. Method of measurement: Oswestry Disability Index.;Quality of Life. Timepoint: At the start of the trial, five days later, ten days later, and one month afterwards. Method of measurement: Functional rating index.;Blood pressure. Timepoint: At the start of the trial, five days later, ten days later, and one month afterwards. Method of measurement: Sphygmomanometer.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Shahbazi

Mashhad University of Medical Sciences

shahbazim2@mums.ac.ir+98 51 3884 6710

Outcome results

None listed

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