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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05467878
Other study ID # SBÜ Bursa Hastanesi
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2021
Est. completion date January 15, 2022

Study information

Verified date July 2022
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date January 15, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - patient giving consent - accessing patient information Exclusion Criteria: - missing information in the patient file

Study Design


Related Conditions & MeSH terms


Intervention

Other:
The 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.

Locations

Country Name City State
Turkey Bursa YIEAH Bursa Yildirim

Sponsors (1)

Lead Sponsor Collaborator
Tugba Onur

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analog Scala (VAS) 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.
1 days after the surgery
Secondary Hospital stay The time elapsed from the patients to the discharge after the operation will be recorded from the files as hours. after the surgery to the discharge time until 10 days
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