Does Adding Posterior Block to SFIB Increase the Quality of Analgesia in Hip Fractures?

NCT ID: NCT06839742

Last Updated: 2026-01-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-24

Study Completion Date

2025-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The researchers aimed to compare the effects of adding a Deep Posterior Gluteal Compartment Block to a Suprainguinal Fascia Iliaca Compartment Block (SFICB) versus SFICB alone on pain, analgesic consumption, and positioning pain for neuraxial anesthesia.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Adding Deep Posterior Gluteal Compartment Block to Suprainguinal Fascia Iliaca Block applied before neuraxial anesthesia in hip fracture surgeries can reduce the pain sensation originating from the posterior region of the hip joint. Thus, participants can experience less pain in the perioperative period, consume less analgesics and reduce complications related to these in the postoperative period. In addition, possible complications can be prevented with early mobilization of the participants. It was aimed to compare the effects of adding Deep Posterior Gluteal Compartment Block to Suprainguinal Fascia Iliaca Block with only Suprainguinal Fascia Iliaca Block on these results.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Acute Pain Management Hip Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Caregivers Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group SFICB

Suprainguinal fascia iliaca plane block will be performed 30 minutes before hip surgery

Group Type ACTIVE_COMPARATOR

Suprainguinal fascia iliaca compartment block

Intervention Type OTHER

Suprainguinal fascia iliaca compartment block will be performed under USG guidance before neuraxial anesthesia.

Group Combined

Suprainguinal Fascia İliaca plane Block will be performed 30 minutes before hip surgery and Deep Posterior Gluteal Compartment Block will be performed 20 minutes before hip surgery

Group Type ACTIVE_COMPARATOR

Deep Posterior Gluteal Compartment Block

Intervention Type OTHER

Deep Posterior Gluteal Compartment Block will be performed under USG guidance before neuraxial anesthesia.

Suprainguinal fascia iliaca compartment block

Intervention Type OTHER

Suprainguinal fascia iliaca compartment block will be performed under USG guidance before neuraxial anesthesia.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Deep Posterior Gluteal Compartment Block

Deep Posterior Gluteal Compartment Block will be performed under USG guidance before neuraxial anesthesia.

Intervention Type OTHER

Suprainguinal fascia iliaca compartment block

Suprainguinal fascia iliaca compartment block will be performed under USG guidance before neuraxial anesthesia.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Volunteering to participate in the study
* Patients between the ages of 18-90
* ASA I, II, III
* Patients whose surgery duration does not exceed 2 hours
* Patients who will undergo surgery under spinal anesthesia

Exclusion Criteria

* Patients who do not want to participate in the study/do not give consent
* Patients with a condition that prevents regional anesthesia
* Patients with cognitive dysfunction who are unable to evaluate the NRS score and who cannot use PCA (Patient Controlled Analgesia Device)
* History of hypersensitivity or allergy to local anesthetics
* Patients with psychiatric disorders and those using psychiatric medications
* Presence of hematological disease
* Presence of oncological disease
* Patients with serious major organ failure
* Presence of multiple fractures
* Patients with alcohol or drug addiction
* Patients who have used analgesic drugs up to 12 hours before surgery
* ASA IV-V patients
* Morbidly obese patients
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Samsun University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

HATİCE SELÇUK KUŞDERCİ

Role: STUDY_DIRECTOR

SAMSUN UNİVERSITY

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Samsun University, Samsun Training and Research Hospital

Samsun, Ilkadım, Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

References

Explore related publications, articles, or registry entries linked to this study.

Safa B, Trinh H, Lansdown A, McHardy PG, Gollish J, Kiss A, Kaustov L, Choi S. Ultrasound-guided suprainguinal fascia iliaca compartment block and early postoperative analgesia after total hip arthroplasty: a randomised controlled trial. Br J Anaesth. 2024 Jul;133(1):146-151. doi: 10.1016/j.bja.2024.04.019. Epub 2024 May 18.

Reference Type BACKGROUND
PMID: 38762396 (View on PubMed)

Roche JJ, Wenn RT, Sahota O, Moran CG. Effect of comorbidities and postoperative complications on mortality after hip fracture in elderly people: prospective observational cohort study. BMJ. 2005 Dec 10;331(7529):1374. doi: 10.1136/bmj.38643.663843.55. Epub 2005 Nov 18.

Reference Type BACKGROUND
PMID: 16299013 (View on PubMed)

Vermeylen K, Van Aken D, Versyck B, Casaer S, Bleys R, Bracke P, Groen G. Deep posterior gluteal compartment block for regional anaesthesia of the posterior hip: a proof-of-concept pilot study. BJA Open. 2023 Feb 15;5:100127. doi: 10.1016/j.bjao.2023.100127. eCollection 2023 Mar.

Reference Type BACKGROUND
PMID: 37587997 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

OMUKAEAK 2024/276

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.