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Clinical Efficacy of Non-Muscle Relaxant General Anesthesia Combined with Transversus Abdominis Plane Block for Laparoscopic Hernia Repair in Pediatric Patients

Clinical Efficacy of Non-Muscle Relaxant General Anesthesia Combined with Transversus Abdominis Plane Block for Laparoscopic Hernia Repair in Pediatric Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097075
Enrollment
Unknown
Registered
2025-02-12
Start date
2025-02-16
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Inguinal hernia

Interventions

Control group:Simple general anesthesia without muscle relaxation group:After the laryngeal mast was inserted, general anesthesia was maintained with sevoflurane(1.0 MAC). After the end of the procedu
Intervention group:General anesthesia without muscle relaxants combined with Transversus Abdominis Plane block: After the laryngeal mast was inserted, general anesthesia was maintained with sevofluran

Sponsors

The Second Affiliated Hospital and Yuying Children's Hospitai of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 6 Years

Inclusion criteria

Inclusion criteria: Aged 1 to 6 years old (under 7 years old); body weight falling within the 25th to 75th percentile range for their corresponding age; classified as American Society of Anesthesiologists (ASA) physical status I or II; scheduled for elective unilateral or bilateral extraperitoneal laparoscopic hernia repair; consented to participate this trial by legal guardians.

Exclusion criteria

Exclusion criteria: Recurrent hernia; history of asthma; potential difficult airway; allergy to anesthetic drugs used in this study; uncorrected severe congenital heart disease; high-risk groups for perioperative respiratory adverse events (such as recent respiratory infection within the past 2 weeks, history of wheezing within the past 12 months, wheezing after activity, nocturnal dry cough, etc.); history of abdominal surgery; preoperative use of analgesics within less than 5 half-lives.

Design outcomes

Primary

MeasureTime frame
Leiden Surgical Rating Scale(L- SRS) Score;—

Secondary

MeasureTime frame
Pediatric Anesthesia Recovery Agitation Scale (PEAD) Score;FLACC Pain Assessment Scale Score;Intraoperative blood pressure;Intraoperative heart rate;Frequency and proportion of intraoperative rescue interventions;Duration of anesthesia;Duration of operation;Incidence of emergence agitation in PACU ;Rate of rescue analgesia with fentanyl in PACU ;PACU stay ;Surgeon‘s’ satisfaction;Perioperative adverse events;—

Countries

China

Contacts

Public ContactKaiming Yuan

The second Affiliated Hospital and Yuying Children's Hospitai of Wenzhou Medical University

yuankm_wh@163.com+86 138 1970 8274

Outcome results

None listed

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