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PENG block and pre-habilitation

Effect of Pericapsular Nerve Group Block in Preoperative Rehabilitation for Patients with Femoral Neck Fracture

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1031220294
Enrollment
100
Registered
2022-08-26
Start date
2022-11-02
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Femoral neck fracture Femoral neck fracture, hip fracture

Interventions

Pericapsular Nerve Group Block using 20ml of 0.375% ropivacaine in intervention group
20ml of saline in control group
PENG block

Sponsors

Sugiyama Daisuke
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients who are 20 years old or older at the time of obtaining the consent form (2) Patients with a Garden stage 3-4 femoral neck fracture who are scheduled artificial head replacement surgery (3) ASA-PS (American Society of Anesthesiologists physical status): 1 (good general condition without complications) to 3 (severe systemic disease but not incapacitated)

Exclusion criteria

Exclusion criteria: (1) Patients with dementia (defined as <3 points in Mini-cog test) (2) Patients with allergies to the investigated drug (3) Patients who could not mobilize before the injury (defined as leaving the bed) (4) Patients with a history of ipsilateral artificial head replacement (5) Patients with infection at the site where PENG block will be performed (6) Patients who have pathological fracture (7) Patients who are judged by the doctor in charge to be inappropriate for participation in this study

Design outcomes

Primary

MeasureTime frame
Success rate of mobilization in the initial preoperative rehabilitation (defined as transferring to a wheelchair with the assistance of a physical therapist)

Secondary

MeasureTime frame
(1) Achievement of the following rehabilitation items in the initial rehabilitation (total of 5 items; 1 point if achieved, 0 point if not achieved, full score of 5 points; under the assistance of a physical therapist): 1) Bed sitting position 2) Edge sitting position 3) Stand up 4) Maintaining a standing position (holding a standing position for 10 seconds with support for unloading the affected leg using a walker) 5) Wheelchair transfer (2) NRS (pain score) at the time of implementation of each item (3) Level of achievement of rehabilitation after the second preoperative session (4) Preoperative hemoglobin (5) Intraoperative blood loss amount (6) Complications within 1 week after surgery (thromboembolic event) (7) POD3 Cumulated Ambulation Score (CAS; score that predicts postoperative patient's motor function; correlates with postoperative outcome) (8) Achievement of postoperative rehabilitation using the protocol shown in (1) (9) Required number of days for each postoperative rehabilitation item (10) Discharge time (11) Discharge destination (home, rehabilitation hospital, facility, unable to transfer hospital, etc.) (12) Half year mortality, ADL

Contacts

Public ContactZhuan Jin

Kameda Medical Center

jin.zhuan@kameda.jp+81-4-7092-2211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026