Skip to content

Application of Pericapsular Nerve Group (PENG) Block

Application of Pericapsular Nerve Group (PENG) Block in Transurethral Resection of Bladder Tumors

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07078773
Enrollment
68
Registered
2025-07-22
Start date
2025-07-12
Completion date
2026-12-31
Last updated
2025-08-13

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

Conditions

TURBT

Keywords

Pericapsular Nerve Group (PENG) block, obturator nerve reflex

Brief summary

This study aims to determine the efficacy and safety of the Pericapsular Nerve Group (PENG) block in preventing obturator nerve reflex during transurethral resection of bladder tumors.

Detailed description

During transurethral resection of bladder tumors (TURBT), obturator nerve reflex is easily triggered during electrocautery. Currently, two primary methods are used to prevent obturator nerve reflex: deep neuromuscular blockade under general anesthesia and obturator nerve block. To date, no studies have confirmed the efficacy of the Pericapsular Nerve Group (PENG) block in preventing obturator nerve reflex. This study recorded the percentage decrease in adductor muscle strength at various time points after the PENG block, the occurrence of intraoperative adductor muscle spasms, the duration of nerve block procedure, and the incidence of postoperative adverse events. The completion of this study could provide clinical evidence for selecting anesthesia methods in TURBT procedures and offer robust evidence-based support for relevant medical decisions by government health agencies.

Interventions

PROCEDUREpeng block

A convex ultrasound probe (frequency 2-5 MHz) was positioned at the patient's inguinal ligament, with one end directed toward the anterior inferior iliac spine (AIIS), clearly visualizing the bony prominences of the iliopubic eminence and the AIIS. The needle tip was directed medially toward the pectineus muscle. Upon reaching the space between the pectineus muscle and the pubic bone, and after confirming the absence of blood on aspiration, 30 ml of 0.375% ropivacaine was injected.

An ultrasound probe was positioned at the inguinal ligament, with the needle inserted parallel to the long axis of the probe. After confirming no blood upon aspiration, 15 ml of 0.375% ropivacaine was injected into the fascial plane between the adductor brevis and adductor magnus, as well as into the midportion of the adductor longus and adductor brevis muscles.

Sponsors

Nanjing First Hospital, Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18 years or older; * Scheduled for TURBT for unilateral bladder tumor; * Able to understand and provide informed consent;

Exclusion criteria

* Patients who refuse or are unable to provide informed consent; * Allergic to local anesthetics, insensitive to propofol or general anesthetics; * Pregnant women; * Severe liver dysfunction; * Evidence of infection at or near the proposed puncture site; * Any sensory or motor impairment of the lower limbs; * Recent (within 6 months) lower limb joint replacement surgery.

Design outcomes

Primary

MeasureTime frameDescription
the percentage reduction in adductor muscle strength at 5, 10, 15, 20, 25, 30 minutes, and 3 hours after drug administration, compared to pre-administration levels.5, 10, 15, 20, 25, 30 minutes, and 3 hours post-administrationThe percentage increase in adductor strength from preoperative to postoperative measurements divided by preoperative adductor strength is larger, reflecting a better nerve block effect and superior obturator nerve reflex inhibition.

Secondary

MeasureTime frameDescription
Presence of obturator nerve reflex during surgeryDuring surgeryObturator nerve reflex grading system: No response in the adductor muscle group of the thigh; mild muscle twitching in the adductor muscle group of the thigh; severe contraction of the adductor muscle group of the thigh

Other

MeasureTime frameDescription
Surgical DurationDuring surgeryIndirectly reflects interference from obturator nerve reflex; shorter duration implies effective reflex suppression
Needle Pass CountDuring nerve block proceduresFewer passes indicate simpler operation and higher precision.
Physician Satisfaction ScoreUp to 48 hours postoperativeGrading: Excellent (1 point) Good (2 points) Fair (3 points) Poor (4 points) Higher scores indicate superior inhibition of obturator nerve reflex and better block efficacy
Patient Satisfaction Score Patient Satisfaction Score Patient Satisfaction ScoreUp to 48 hours postoperativeGrading: Excellent (1 point) Good (2 points) Fair (3 points) Poor (4 points) Higher scores reflect enhanced patient comfort during the procedure
Operational Duration of Nerve BlockDuring nerve block proceduresReflects procedural convenience; shorter duration indicates simpler technique
Incidence of adverse reactions such as local anesthetic toxicity and nerve injury post-administration.Up to 48 hours postoperativeThe lower the incidence of adverse reactions such as local anesthetic toxicity and nerve injury, the better the PENG block technique. quantifies safety profile (lower incidence indicates higher safety)

Countries

China

Outcome results

None listed

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