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Clinical Trials in Turkey / NCT07612761
Recruiting Observational

Comparison of Meta-PENG and Suprainguinal Fascia Iliaca Plane Block in Hip Fractures

NCT07612761 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-05-14
Last updated
2026-05-29

Condition(s) studied

Hip FracturePostoperative PainRegional Anesthesia

Investigational drug(s) / intervention(s)

Ultrasound-Guided Meta-PENG BlockUltrasound-Guided Suprainguinal Fascia Iliaca Plane Block

Ultrasound-Guided Meta-PENG Block: Ultrasound-guided meta-PENG block performed as part of routine perioperative regional analgesia management in patients undergoing hip fracture surgery under spinal anesthesia.

Ultrasound-Guided Suprainguinal Fascia Iliaca Plane Block: Ultrasound-guided suprainguinal fascia iliaca plane block performed as part of routine perioperative regional analgesia management in patients undergoing hip fracture surgery under spinal anesthesia.

Study summary

This prospective observational single-center study will compare the effects of ultrasound-guided meta-PENG block and suprainguinal fascia iliaca plane block in patients undergoing hip fracture surgery under spinal anesthesia.

Hip fracture surgery can cause significant pain before, during, and after the operation. Regional anesthesia techniques may help reduce pain, improve positioning for spinal anesthesia, decrease the need for additional analgesics, and support earlier mobilization.

Patients included in the study will be adults scheduled for hip fracture surgery under spinal anesthesia. According to routine clinical practice and the anesthesiologist's decision, patients will receive either ultrasound-guided meta-PENG block or ultrasound-guided suprainguinal fascia iliaca plane block. The study will not assign patients to a treatment group by randomization.

The main outcome will be pain during positioning for spinal anesthesia, measured using the Numeric Rating Scale. Additional outcomes will include postoperative pain at rest and during activity, additional analgesic consumption, patient satisfaction, mobilization time, and length of hospital stay.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age greater than 18 years * ASA physical status I-III * Scheduled to undergo hip fracture surgery under spinal anesthesia * Written informed consent obtained from the patient or the patient's legal representative Exclusion Criteria: * Refusal to participate in the study * ASA physical status IV-V * Presence of central or autonomic nervous system disease * Known allergy to the drugs used in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sancaktepe Sehit Prof. Dr. Ilhan Varank Training and Research Hospital Istanbul Istanbul Recruiting

More Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital trials in Turkey

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07612761 on ClinicalTrials.gov ↗ ← All trials in Turkey