Health TrialsbyHealthPanel

Effects of Pericapsular Nerve Group Block Applied in Patients Undergoing Hip Fracture Surgery.

ConditionsHip FracturesPain, Postoperative
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-85
SponsorUmraniye Education and Research Hospital

About this trial

In this study, it was aimed to compare the multimodal analgesia application or the pericapsular nerve group (PENG) block methods in patients undergoing hip surgery. The effectiveness and benefit rate of the PENG block in postoperative pain will be evaluated.

Postoperative pain, need for additional analgesia, range of motion of the hip joint, mobilization time, length of hospital time and adverse events in patients undergoing hip fracture surgery with and without PENG block will be investigated.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients who will undergo hip fracture surgery Women and men aged 30-85

Disqualifiers

Patients under 30 years old, over 85 years old

American Society of Anesthesiology (ASA) IV,

Those with cognitive impairment (alzheimer, dementia, delirium, etc.)

Those with application site infection

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pericapsular Nerve Group (PENG) Block

    Procedure/Surgery

    Pericapsular nerve group (PENG) block The femoral nerve and obturator nerve terminal branches, which provide sensory innervation of the hip joint, are blocked, thus providing analgesia without creating a motor block.

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: PENG Block groupActive comparator 1 intervention
Group B: Control groupOther 1 intervention

Trial outcomes

Primary outcomes

1

postoperative pain score

VAS pain score

Time frame
30 min, 12th, 24th and 48th hours in the postoperative period
2

Total opioid consumption

Tramadol (mg)

Time frame
postoperative 48 hours
3

mobilisation time

take 5 steps with walker

Time frame
postoperative 24-48 hours

Secondary outcomes

1

PENG block adverse events

motor block, nerve damage, hypotension, bradycardia

Time frame
between the time surgery starts and the 48th hour
2

length of hospital stay

day

Time frame
between the time of hospitalization for the operation and discharge (day)

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Umraniye Education and Research Hospital

Lead sponsor

Source ClinicalTrials.gov
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