Comparison of the Analgesic Effectiveness of Pericapsular Nerve Block and Suprainguinal Fascia Iliac Block Application

ConditionHip Surgery
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorTC Erciyes University

About this trial

Suprainguinal Fascia iliac compartment outlet and Pericapsular nerve reduction, which is a routinely successful method for postoperative analgesia in anesthesia practice; the aim is to investigate information regarding postoperative pain level, analgesic consumption, patient satisfaction and discharge time after arm arthroscopy.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients over the age of 18 and under the age of 65 who will undergo hip arthroscopy

ASA I-II group patients

Patients without allergies

Patients without psychiatric disorders

Disqualifiers

Patients who do not want to participate in the study

Patients with uncontrolled hypertension

Patients with chronic pain or receiving pain treatment,

Significant Cardiac Disorder (Coronary Artery Disease, Arrhythmia, Electrocardiography Anomaly, Heart Failure, etc.)

Trial population

Patients over the age of 18 and under the age of 65 who will undergo hip arthroscopy

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

60 Participants
are grouped into 2 trial groups
Group A: Pericapsular Nerve Block (PENG)
Group B: Suprainguinal Fascia Iliaca Block (SFIB)

Trial outcomes

Primary outcomes

1

Visual Analogue Score

A Visual Analogue Scale (VAS) is one of the pain rating scales. It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms. For example, the amount of pain that a patient feels ranges across a continuum from none to an extreme amount of pain. From the patient's perspective, this spectrum appears continuous; their pain does not take discrete jumps, as a categorization of none, mild, moderate and severe would suggest the VAS score for grading of pain consists of a 10 centimetres (cm) line with 10 mm (0.01 cm) to each point of the scale and two end-points representing no pain and worst possible pain, where 0 = no pain, 1-3 = mild, 4-6 = moderate and 7-10 = severe pain

Time frame
2-3 hours after surgery

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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