Does apprehension before injection for back pain predict response in patients with back pain radiating to leg

Does pre procedural anxiety predict outcome after epidural steroid injections in patients with radicular lumbosacral pain? A prospective correlational study.

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2021/04/032699

Enrollment

100

Registered

2021-04-09

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: M472- Other spondylosis with radiculopathy

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: patients with radicular lumbosacral pain of atlas 3 months not responding to physical and medical therapies

Exclusion criteria

Exclusion criteria: local infection at block site coagulopathy morbid obesity BMI >40 allergy to local aesthetics preexisting neurological deficits with significant cognitive dysfunction and diagnosed psychiatric disorder mental retardation failed back surgery.

Design outcomes

Primary

Measure	Time frame
Correlation between pre procedural anxiety and effective pain relief at various periods of follow upTimepoint: 3 months post procedure	—

Secondary

Measure	Time frame
1. Incidence of anxiety 2. Mean preprocedural anxiety scores 3. Number of attempts for procedure 4. Performerâ??s satisfaction score 5. Average buttock/hip/leg pain intensity using VAS at baseline and 2 weeks, 3 weeks 6weeks , 10 weeks and 14 weeks after the injection. 6. Disability using Roland-Morris Disability Questionnaire at baseline Timepoint: 2 weeks, 4 weeks, 6weeks , 10 weeks and 14 weeks after the injection	—

Measure

Time frame

1. Incidence of anxiety 2. Mean preprocedural anxiety scores 3. Number of attempts for procedure 4. Performerâ??s satisfaction score 5. Average buttock/hip/leg pain intensity using VAS at baseline and 2 weeks, 3 weeks 6weeks , 10 weeks and 14 weeks after the injection. 6. Disability using Roland-Morris Disability Questionnaire at baseline Timepoint: 2 weeks, 4 weeks, 6weeks , 10 weeks and 14 weeks after the injection

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Countries

India

Contacts

Public ContactDr Jeetinder Kaur Makkar

PGIMER, CHANDIGARH

jeet1516@gmail.com7087009510

Outcome results