Nephrectomy Clinical Trials

Clinical trials related to Nephrectomy Procedure

Effect of Preoperative Active Prewarming on Serum Lactate Levels and Perioperative Outcomes in Patients Undergoing Elective Nephrectomy: A Prospective Observational Study

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

The goal of this observational study is to learn whether warming patients before surgery, called prewarming, affects blood lactate levels (a marker of how well tissues are getting oxygen) and recovery in adults having planned (elective) kidney removal surgery (nephrectomy). The main questions this study aims to answer are: * Does prewarming lower the rise in blood lactate seen during and after surgery? * Does prewarming affect time spent in the intensive care unit (ICU), the need for a blood transfusion, or the rate of complications after surgery? Researchers will compare two groups of adults having this surgery. One group receives brief active warming before anesthesia (the prewarming group). The other group does not receive this warming (the control group). The anesthesia team decides whether to use prewarming and for how long, as part of routine care; the study does not change this decision. Researchers will compare the two groups to see whether prewarming is linked to lower lactate levels and better recovery. Participants will: * Receive their usual, routine surgery and anesthesia care * Have blood pressure, heart rate, body temperature, and blood tests, including lactate, checked before and after surgery, as already done in routine care * Have their ICU stay, need for blood transfusion, and any complications recorded This study does not add any extra tests, procedures, or blood draws beyond routine clinical care.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

• Scheduled for elective nephrectomy

• Adults aged 18-90 years

• ASA (American Society of Anesthesiologists) physical status classification I-III

• Signed informed consent form

Locations
Other Locations
Turkey
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
RECRUITING
Istanbul
Time Frame
Start Date: 2025-11-15
Estimated Completion Date: 2026-11-15
Participants
Target number of participants: 128
Treatments
Prewarming Group
Patients who receive active preoperative warming, applied by the anesthesia team during operating room preparation, typically for approximately 10-15 minutes before induction of anesthesia, as part of routine clinical care.
Control Group
Patients who do not receive active preoperative warming before induction of anesthesia, per the routine practice of the anesthesia team providing care. All patients receive standard intraoperative and postoperative warming per usual care.
Related Therapeutic Areas
Sponsors
Leads: Beyzanur Aydoğdu

This content was sourced from clinicaltrials.gov