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Neural Therapy in Notalgia Paresthetica

Neural Therapy in Notalgia Paresthetica

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06508073
Enrollment
12
Registered
2024-07-18
Start date
2024-06-26
Completion date
2024-07-10
Last updated
2024-07-18

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

Conditions

Notalgia Paresthetica

Keywords

back pain, intralesional injection, neuralgia, pruritus

Brief summary

Patients diagnosed with Notalgia paresthetica and who received neural therapy within the last year were retrospectively screened. In the evaluations before treatment and at the 3rd month after treatment; Numerical rating scale for pain, PainDETECT questionnaire for neuropathic pain, SF-12 for quality of life and 5-D itch scale for itch level were used.

Interventions

The injection was prepared using a solution of lidocaine 2% and saline 0.9%. A 0.4% lidocaine solution was prepared by diluting 1 cc of lidocaine with 4 cc of saline.

Sponsors

Sisli Hamidiye Etfal Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* the presence of a hyperpigmented skin lesion consistent with NP * minimum 6 months for duration of disease * 30-60 aged * application of neural therapy in a manner appropriate to the diagnosis

Exclusion criteria

* history of previous surgery or injection in the thoracic region * presence of another treatment in the same period * presence of any cardiac or pulmonary disease, malignancy, or advanced psychiatric disease

Design outcomes

Primary

MeasureTime frameDescription
Numeric Rating Scale for Pain12 weeks after treatmentA scale between 0 and 10 was used to question the pain level.
PainDETECT Questionnaire for assessing Neuropathic pain12 weeks after treatmentThe questionnaire consists of 9 items and is completed by the patient (no clinical examination is required)\[1\]\[3\]. There are 7 weighted sensory descriptor items (never to very strongly) and 2 items relating to spatial and temporal pain characteristics\[3\]. A total score of 19 or more is indicative of likely neuropathic pain.
Short Form-12 for Quality of life12 weeks after treatmentThe SF-12 is a self-reported outcome measure assessing the impact of health on an individual's everyday life. It is often used as a quality of life measure.
5-D Itch Scale12 weeks after treatmentThe 5-D itch scale is a 5-domain disease-specific instrument evaluating the duration, degree (severity), direction (improving, unaltered or worsening), disability (impact on sleep, leisure/social, housework/errands and school/work activities) and distribution (body part affected)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026