Perioperative analgesia in pediatric laparoscopic herniorrhaphy surgery: a comparison of three different concentrations of ropivacaine for TAP block

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-14004602

Enrollment

Unknown

Registered

2014-05-04

Start date

2014-06-04

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

pediatric hernia

Interventions

the control group:saline for TAP block

0.0625% ropivacaine group:0.0625% concentrations of ropivacaine for TAP block

0.125% ropivacaine group:0.125% concentrations of ropivacaine for TAP block

0.25% ropivacaine group:0.25% concentrations of ropivacaine for TAP block

Eligibility

Sex/Gender

Male

Age

1 Years to 3 Years

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists physical status I–II patients aged between 1 years and 3 years developed normally boys with primary inguinal hernia scheduled for selective Pediatric laparoscopic High Ligation of Inguinal Hernia ambulatory Surgery were eligible to participate in the study.

Exclusion criteria

Exclusion criteria: Patients were excluded if regional block refusal, known amide local anesthetic drug allergy and Operation site infection, or the patient was assessed as block failure.

Design outcomes

Primary

Measure	Time frame
postoperative analgesia and sedation;	—

Secondary

Measure	Time frame
Intraoperative haemodynamic profile;peroperative additional analgesics that were required;parental satisfaction;side-effect;	—

Countries

China

Contacts

Public ContactLing Tan

West China Hospital, Sichuan University

scutanl@163.com+86 18980601546

Outcome results

None listed

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