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Clinical study of transcranial magnetic stimulation to improve sexual dysfunction in male patients after percutaneous endoscopic lumbar disc nucleus pulposus extraction

Clinical study of transcranial magnetic stimulation to improve sexual dysfunction in male patients after percutaneous endoscopic lumbar disc nucleus pulposus extraction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091582
Enrollment
Unknown
Registered
2024-10-30
Start date
2024-11-05
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Lumbar disc herniation, erectile dysfunction

Interventions

PELD+TMS:PELD+TMS
PELD+sham TMS:PELD+sham TMS

Sponsors

Hangzhou First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients receiving PELD; 2. Patients with fixed sexual partners and sexual history of 6 months or more after LDH had IIEF-5 scores decreased to varying degrees; 3. The level of sex hormones is within the normal range; 4. No diabetes or diabetes but no peripheral neuropathy; 5. No history of mental illness or family history of mental illness; 6. No history of perineal nerve injury; 7. No recent use of drugs to inhibit penile erection; 8. Normal development of penis and testicles.

Exclusion criteria

Exclusion criteria: 1. Previous history of cervical and lumbar surgery; 2. Patients with pelvic autonomic plexus injury; 3. Compression of cauda equina nerve in the anus perineal area causing paresthesia or sexual dysfunction; 4. Severe postoperative complications; 5. Widowed or without a permanent sexual partner; 6. Malformations of the reproductive system; 7. Suffering from serious heart and brain disorders; 8. Previous history of epileptoid seizures/seizures/taking antiepileptic drugs; 9. Patients who have undergone brain surgery for stroke or other reasons; 10. Metal implantation (e.g., cardiac pacemaker, spinal cord stimulator, vascular stent, fracture internal plate, etc.); 11. Unwilling to cooperate with the experiment.

Design outcomes

Primary

MeasureTime frame
Erectile function;

Secondary

MeasureTime frame
Oswestry Disability Index Questionnaire (ODI);Visual Analog Scale;Depression;Anxiety;plasma proteins;plasma metabolites;inflammatory factors;

Countries

China

Contacts

Public ContactHanbin Wang

Hangzhou First People's Hospital

458154923@qq.com+86 15757119331

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026