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Developing a Clinical Prediction Model for Adverse Outcomes in Percutaneous Trigeminal Ganglion Balloon Compression

A

Affiliated Hospital of Nantong University

Status

Completed

Conditions

Trigeminal Neuralgia (TN)

Study type

Observational

Funder types

Other

Identifiers

NCT06998420
2024-K098-01

Details and patient eligibility

About

This clinical study aims to investigate adverse outcomes following percutaneous balloon compression (PBC) of the trigeminal ganglion, establish a predictive model, and assess the probability of postoperative complications.The main question it aims to answer is:

  1. What factors are associated with adverse postoperative outcomes?
  2. What is the occurrence probability of different types of adverse outcomes? The study will record patients' demographic and clinical characteristics, laboratory test results, and conduct follow-ups at 3, 6, and 12 months postoperatively.

Enrollment

110 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Diagnosed with primary trigeminal neuralgia and underwent PBCG at the Pain Department of Affiliated Hospital of Nantong University
  2. Age ≥18 years
  3. Willing to complete postoperative follow-up

Exclusion criteria

  1. Secondary trigeminal neuralgia (e.g., tumor compression, multiple sclerosis)
  2. Previous interventional treatments for trigeminal neuralgia
  3. Incomplete follow-up data
  4. General anesthesia contraindications or significant dysfunction of major organs (cardiac, pulmonary, hepatic, renal) or severe neurological impairment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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