Health TrialsbyHealthPanel

Postoperative Analgesia Practices After Percutaneous Nephrolithotomy

ConditionNephrolithiasis
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorIstinye University

About this trial

This prospective observational study aims to evaluate the effectiveness and safety of different postoperative analgesia methods used in patients undergoing percutaneous nephrolithotomy (PCNL). Analgesia techniques are determined independently by the responsible anesthesiologist as part of routine clinical practice, and the study team does not intervene in treatment decisions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults aged 18-65 years

ASA physical status I-III

Undergoing unilateral PCNL

Providing written informed consent

Disqualifiers

Known allergy to local anesthetics

Trial population

Adult patients aged 18 to 65 years undergoing unilateral percutaneous nephrolithotomy (PCNL) at Haseki Training and Research Hospital. All participants are ASA physical status I-III and receive postoperative analgesia according to routine clinical practice.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

75 Participants
are grouped into 3 trial groups
Group A: quadro iliac plane block
Group B: erector spinae nerve block
Group C: Intravenous opioid-based analgesia

Trial outcomes

Primary outcomes

1

Cumulative opioid consumption

Cumulative opioid consumption in the first 24 hours

Time frame
24 hours

Secondary outcomes

1

Pain scores at rest and during movement

Pain intensity measured using the Numeric Rating Scale (NRS), a validated 11-point pain scale ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst pain imaginable. Higher scores represent worse pain

Time frame
0, 2, 6, 12, and 24 hours postoperatively
2

Time to first analgesic request

Time to first analgesic request

Time frame
Postoperative 24 hours
3

Need for rescue analgesics

Need for rescue analgesics

Time frame
24 hours
4

Intraoperative opioid consumption

Intraoperative opioid consumption

Time frame
During surgery

Other outcomes

Sponsors and contacts

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

Istinye University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: