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The application of different concentrations of ropivacaine for penile root nerve block in postoperative analgesia of pediatric urological urethral surgery

The application of different concentrations of ropivacaine for penile root nerve block in postoperative analgesia of pediatric urological urethral surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088354
Enrollment
Unknown
Registered
2024-08-16
Start date
2024-08-31
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Hypospadias

Interventions

0.1% concentration of ropivacaine group:Dorsal penile nerve block is performed under ultrasound guidance using 0.1% concentration of ropivacaine
0.15% concentration of ropivacaine group:Dorsal penile nerve block is performed under ultrasound guidance using 0.15% concentration of ropivacaine
0.2% concentration of ropivacaine group:Dorsal penile nerve block is performed under ultrasound guidance using 0.2% concentration of ropivacaine

Sponsors

Shengjing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
No minimum to 12 Years

Inclusion criteria

Inclusion criteria: (1) Age 0~12 years old; (2) Children undergoing elective urethral surgery; (3) American Society of Anesthesiology (ASA) grade I-II; (4) Children who are scheduled to undergo elective surgery and use tracheal intubation (ordinary cuffed catheter) or laryngeal mask as the main anesthetic airway management method; (5) Informed consent of the guardian and signing of the informed consent form.

Exclusion criteria

Exclusion criteria: (1)Younger than 3 months or older than 12 years old; (2)Mallampati Airway Grading >Class II; (3)Infection or redness and swelling at the injection site; (4)Respiratory malformations, foreseeable difficulties in the airway; (5)Neurological deficits, bleeding disorders; (6)Patients with a recent history of upper respiratory tract infection; (7)History of local anesthetic allergy; (8)Obesity (BMI=30kg/m2) or malnutrition(BMI=18.5kg/m2).

Design outcomes

Primary

MeasureTime frame
FLACC pain score;VAS-P anxiety score in preoperative families;Postoperative family gas-pop anxiety score;

Secondary

MeasureTime frame
Additional analgesic medication timing and dosage are required;Duration of surgery;Postoperative analgesic pump use;Anesthesia-inducing drug dose;heart rate;Blood pressure;Oxygen saturation;

Countries

China

Contacts

Public ContactHan Guang

Shengjing Hospital of China Medical University

849464050@qq.com+86 189 4025 8839

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026