NCT06995079

Brief Summary

The aim is to demonstrate that lumbar ESP block provides more effective postoperative analgesia than PENG block in geriatric patients with hip fractures, and reduces postoperative opioid consumption more than PENG block

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 7, 2025

Completed
22 days until next milestone

First Posted

Study publicly available on registry

May 29, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

June 1, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2026

Completed
Last Updated

May 29, 2025

Status Verified

May 1, 2025

Enrollment Period

5 months

First QC Date

May 7, 2025

Last Update Submit

May 28, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • postoperative pain

    To evaluate postoperative pain after two different block applications in patients undergoing hip fracture surgery.Evaluation of patients' postoperative 30th minute, 2nd hour, 6th hour, 12th hour and 24th hour verbal analog scores.To examine the total fentanyl consumption, acetaminophen consumption, and nonsteroidal anti-inflammatory drug consumption of patients in the postoperative 24 hours.

    6 month

Study Arms (2)

pericapsular nerve group block (peng block)

EXPERIMENTAL

The patient will first be taken to the block room in the operating room.In this group, patients will be given a Peng block before surgery.The patient will then be taken to the operating room and spinal anesthesia will be applied.Postoperative analgesia requirement will be assessed

Procedure: Postoperative pain assessment of patients who underwent block

lumbar erector spinae plane block(lesp block)

EXPERIMENTAL

The patient will first be taken to the block room in the operating room.In this group, patients will be given a lumbar erector spinae plane block before surgery.The patient will then be taken to the operating room and spinal anesthesia will be applied.Postoperative analgesia requirement will be assessed

Procedure: Postoperative pain assessment of patients who underwent block

Interventions

Postoperative pain assessment of patients who underwent block

lumbar erector spinae plane block(lesp block)pericapsular nerve group block (peng block)

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • patients with hip fractures
  • over 65 years old

You may not qualify if:

  • long-term surgery
  • Patients who do not want regional anesthesia
  • bleeding disorder disease
  • wound in the operation area

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 7, 2025

First Posted

May 29, 2025

Study Start

June 1, 2025

Primary Completion

November 1, 2025

Study Completion

January 1, 2026

Last Updated

May 29, 2025

Record last verified: 2025-05