NCT06169462

Brief Summary

Ultrasound-guided Supra-inguinal Fascia Iliaca compartment Block (SIFCB) and Pericapsular Nerve Group Block (PENG) are increasingly being used for postoperative analgesia for hip surgery. The postoperative analgesic efficacy of SIFCB added to PENG block in elderly hip fracture patients will be evaluated. Postoperative opioid consumption and quality of recovery will also be evaluated.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
38

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 31, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2023

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

November 21, 2023

Completed
19 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 10, 2023

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 13, 2023

Completed
Last Updated

December 14, 2023

Status Verified

December 1, 2023

Enrollment Period

7 months

First QC Date

November 21, 2023

Last Update Submit

December 13, 2023

Conditions

Keywords

AnesthesiaLower extremitypericapsular nerve group blocksuprainguinal fascia compartment block

Outcome Measures

Primary Outcomes (1)

  • Opioid consumption

    If the patient's Numerical Rating Scale (NRS) score is equal to or above 4, tramadol 50 mg IV or oxycodone 5 mg orally every 4 hours will be administered as rescue analgesia.

    Postoperative 48th hour

Secondary Outcomes (4)

  • Numerical Rating Scale (NRS) scores

    Postoperative 48th hour

  • Quality of Recovery 15 Score

    Postoperative day 1 and 1 month

  • Postoperative complications

    24 hours

  • Mobilization time

    24 hours

Study Arms (2)

Pericapsular nerve group (PENG) block

Patients who underwent PENG in Hip surgery under spinal anesthesia will be evaluated retrospectively in terms of opioid consumption and NRS scores.

Procedure: PENG block

Suprainguinal fascia compartment block (SIFCB) + PENG

Patients who underwent PENG+SIFCB in Hip surgery under spinal anesthesia will be evaluated retrospectively in terms of opioid consumption and NRS scores.

Procedure: PENG block+ SIFCB

Interventions

PENG blockPROCEDURE

Patients underwent ultrasound-guided PENG Block for older adult patients surgery for hip fracture. Patients who received opioids as a rescue analgesic during postoperative pain management on selected dates will be included in the study.

Also known as: Drug
Pericapsular nerve group (PENG) block

Patients underwent ultrasound-guided PENG Block+ SIFCB for older adult patients surgery for hip fracture. Patients who received opioids as a rescue analgesic during postoperative pain management on selected dates will be included in the study.

Also known as: Drug
Suprainguinal fascia compartment block (SIFCB) + PENG

Eligibility Criteria

Age65 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Data of patients underwent hip surgery under spinal anesthesia between 31.01.2023 and 01.10.2023.

You may qualify if:

  • Physical status according to American Society of Anesthesiologists (ASA ) I-III

You may not qualify if:

  • Previous operation on the same hip
  • Hepatic or renal insufficiency
  • Patients undergoing general anesthesia
  • Allergy or intolerance to one of the study medications
  • BMI \>40
  • ASA IV

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Karaman Training and Research Hospital

Karaman, Karaman/Merkez, 70200, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Hip Fractures

Interventions

Pharmaceutical Preparations

Condition Hierarchy (Ancestors)

Femoral FracturesFractures, BoneWounds and InjuriesHip InjuriesLeg Injuries

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 21, 2023

First Posted

December 13, 2023

Study Start

January 31, 2023

Primary Completion

September 1, 2023

Study Completion

December 10, 2023

Last Updated

December 14, 2023

Record last verified: 2023-12

Locations