The Effect of Anesthesia on Pain in Percutaneous Nephrolithotomy

The Effect of Anesthesia on Perioperative Pain Level and Analgesic Effect in Patients With Percutaneous Nephrolithotomy

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05467878

Enrollment

500

Registered

2022-07-21

Start date

2021-03-01

Completion date

2022-01-15

Last updated

2022-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Percutaneous Nephrolithotomy

Keywords

general anesthesia, postoperative pain

Brief summary

It is aimed to determine the ideal application by determining the effect of different anesthesia methods applied in percutaneous nephrolithotomy surgeries on analgesic consumption and pain level.

Detailed description

Different anesthesia methods are used in percutaneous nephrolithotomy.In addition to traditional analgesia methods such as intravenous paracetamol, NSAIDs, opioids, various methods such as epidiural analgesia or blocks added to general anesthesia are used.In this study, it was aimed to investigate whether central or peripheral block applications are preferred in percutaneous nephrolithotomy, and the need for intraoperative and postoperative analgesics in patients.In addition, it was aimed to investigate whether there was a change in analgesic consumption, recovery and pain level, and hospital stay in patients who were given general anesthesia or regional anesthesia, in a multicentric observational manner.

Interventions

OTHERThe anesthesia and analgesia technique preferred by the anesthetist will be recorded.

In the study, the anesthesia method applied by blind anesthesiologists in the peroperative period, the drugs or techniques used for analgesia will be recorded and their effects on the postoperative period and hospital stay will be examined.There will be no intervention in the perioperative and postoperative process.

Study design

Observational model

CASE_CONTROL

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

Healthy volunteers

Yes

Inclusion criteria

* patient giving consent * accessing patient information

Exclusion criteria

* missing information in the patient file

Design outcomes

Primary

Measure	Time frame	Description
Visual Analog Scala (VAS)	1 days after the surgery	Postoperative pain levels with Visual analog Scale (VAS):Between 0 and 10 points is chosen by the patients. 0 is no pain, 10 is excessive pain.

Secondary

Measure	Time frame	Description
Hospital stay	after the surgery to the discharge time until 10 days	The time elapsed from the patients to the discharge after the operation will be recorded from the files as hours.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026