The Effect of Anesthesia on Pain in Percutaneous Nephrolithotomy
NCT ID: NCT05467878
Last Updated: 2022-07-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
500 participants
OBSERVATIONAL
2021-03-01
2022-01-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Postoperative Analgesia Practices After Percutaneous Nephrolithotomy
NCT07258901
Comparison Of Epidural Analgesia Techniques In Percutaneous Nephrolithotomy With Surgical Pleth Index
NCT05572164
Comparison of Erector Spinae Plane Block and Intravenous Analgesic in Nefrectomy
NCT04686890
Anterior Quadratus Lumborum Block Versus Erector Spina Plane Block in Percutaneous Nephrolithotomy Surgery
NCT05822492
The Effectiveness of Quadro İliac Plane Block in Percutaneous Nephrolithotomies
NCT07203859
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group I
Patients undergoing regional anesthesia were studied. It can be in the form of combined spinal epidural or epidural anesthesia.
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.
Group 2
Patients in whom general anesthesia and iv analgesic methods are preferred are in this group.
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.
Group 3
Patients who prefer peripheral block under general anesthesia and ultrasound are in this group.
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.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* accessing patient information
Exclusion Criteria
18 Years
80 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Tugba Onur
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Tugba Onur
Medical Doctor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Şeyda Efsun ŞE Özgünay, Assoc Prof
Role: PRINCIPAL_INVESTIGATOR
Bursa Yuksek Ihtisas Training and Research Hospital
Serra S Topal, MD
Role: STUDY_CHAIR
Bursa Yuksek Ihtisas Training and Research Hospital
Sedat S Öner, Assoc Prof
Role: STUDY_CHAIR
Bursa Yuksek Ihtisas Training and Research Hospital
Salim S Zengin, MD
Role: STUDY_CHAIR
Bursa Yuksek Ihtisas Training and Research Hospital
Şermin Ş Eminoğlu, MD
Role: STUDY_CHAIR
Bursa Yuksek Ihtisas Training and Research Hospital
Tuğba T Onur, MD
Role: STUDY_CHAIR
Bursa Yuksek Ihtisas Training and Research Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Bursa YIEAH
Bursa, Yildirim, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SBÜ Bursa Hastanesi
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.