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Anatomical Measurements of Pudendal Nerve Block in Children

Investigation of the Distance of the Needle Entry Point From the Anus and the Depth to Reach the Pudendal Nerve in Pudendal Nerve Block Application in Children

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07348029
Enrollment
50
Registered
2026-01-16
Start date
2026-01-20
Completion date
2026-06-10
Last updated
2026-01-16

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

Conditions

Penile Surgery-Related Pain, Postoperative Pain Management

Keywords

Pudendal Nerve Block, Pediatric Regional Anesthesia, Neurostimulation

Brief summary

This prospective observational study aims to investigate the relationship between anatomical parameters-specifically the distance from the anus to the needle insertion point and the depth required to reach the pudendal nerve-during neurostimulation-guided pudendal nerve block and patients' age, height, and weight in children undergoing penile surgery.

Detailed description

The pudendal nerve originates from the sacral nerve roots Sacral2-Sacral4 and provides sensory and motor innervation to the penile and perineal regions. Effective postoperative analgesia is essential in pediatric penile surgeries. Pudendal nerve block may provide longer-lasting and more effective analgesia compared to caudal or penile blocks. However, due to age- and size-related anatomical variability in children, data regarding optimal needle insertion distance and depth to reach the pudendal nerve are limited. In this study, neurostimulation will be used to confirm pudendal nerve localization, and anatomical measurements will be analyzed in relation to demographic parameters.

Interventions

PROCEDURENeurostimulation-Guided Pudendal Nerve Block

Bilateral pudendal nerve block is performed under general anesthesia with neurostimulation guidance. Anatomical measurements, including distance from anus to needle insertion point and nerve depth, are recorded for each patient. Bupivacaine 0.25% is used at 0.25 ml/kg per side, with a maximum total dose of 2 mg/kg.

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Children aged 1-18 years * Scheduled for penile surgery (e.g., hypospadias, phimosis) * Planned to receive neurostimulation-guided pudendal nerve block * Patient and parents/legal guardians willing to participate under general anesthesia

Exclusion criteria

* Patients with incomplete measurement data * Cases where successful nerve block cannot be performed or nerve stimulation is not detectable at currents ≥1.5 mA * Patients or parents/legal guardians who refuse pudendal nerve block * Patients with pelvic deformities or neuromuscular disorders

Design outcomes

Primary

MeasureTime frameDescription
Horizontal distance from anus to needle insertion point and Depth from skin surface to pudendal nerveDuring pudendal nerve block procedureThe horizontal distance from the anus to the needle insertion point is measured in centimeters for each patient using neurostimulation-guided pudendal nerve block. Measurements are recorded separately for the right and left sides.The depth from the skin surface to the pudendal nerve is measured in centimeters using neurostimulation guidance. Measurements are recorded separately for the right and left sides. The relationship of this distance and the association of nerve depth with patient age, height, and weight will be analyzed.

Countries

Turkey (Türkiye)

Contacts

Primary ContactMunevver Kayhan, Lecturer Doctor
munevver.kayhan@iuc.edu.tr02124143000
Backup ContactPinar Kendigelen, Professor Doctor
pinarken@gmail.com02124143000

Outcome results

None listed

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