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NCT06187883Completed

Pulsed Radiofrequency of Lateral Femoral Cutaneous Nerve

Does Obesity EffectThe Successful Response to the Pulsed Radiofrequency of Lateral Femoral Cutaneous Nerve in Meralgia Parestetica? : A Retrospective Cohort Study

Source: ClinicalTrials.gov · Last updated 22 Apr 2024

Brief summary (registry, in English)

In the current retrospective cohort study, conducted by both pain specialists and neurophysiologists, the primary outcome was to search for the effect of obesity on the efficacy of PRF of LFCN in refractory MP for 6 months. Secondary outcomes were to identify the clinical and diagnostic features of the MP.

Status (registry)
Completed
Study type
Observational
Enrollment
30 (actual)
First submitted
6 Dec 2023
Start date
21 Nov 2023
Primary completion date
30 Nov 2023
Lead sponsor
Mersin Training and Research Hospital
Diseases
Obesity
NCT number
NCT06187883

What you commit to

  • Study type: Observational
  • Participants enrolled: 30
  • From 21 Nov 2023 to the primary completion date, 30 Nov 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • If a new analgesic drug was prescribed during the follow-up period that could affect the evaluation of outcomes, the patients were also excluded.

Other illness

  • Patients with secondary entrapment neuropathy (e.g., diabetes, inflammatory arthritis, hypothyroidism), malignancy, pregnancy, skin infection in the inguinal region or dermatitis, lumbar radiculopathy, polyneuropathy, and cardiac pacemakers were excluded.

Other

  • inadequate follow-up or missing documentation
  • Patients who missed appointments, or were unable to communicate with; were not included in the study.
  • In the SSEP analysis, when the latency of LFCN was not evaluated in both sides, these patients were not also included in the study.

Who the study is looking for

  • older than 18 years treated with PRF neuromodulation of LFCN for MP
  • followed up at least 6 months in the pain clinic of the tertiary hospital between January 2020 and August 2023.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Suna Aşkın Turan
Coordinator of this site? Confirm its status
MersinTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.