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Transversalis Fascia Plane Block and Rectus Sheath Block in Renal Transplantation Donors

Not Applicable
Conditions
Postoperative Pain
Interventions
Procedure: Transversalis fascia plane block and rectus sheath block
Device: Intravenous fentanyl patient control device
Registration Number
NCT05324215
Lead Sponsor
Koc University Hospital
Brief Summary

Transversalis fascia plane block (TFPB) is a relatively new, easy-to-apply and safe regional anesthesia technique used to provide postoperative analgesia in various surgeries. It has been shown that TFPB and rectus sheath block (RSB) administration reduces opioid consumption and related side effects in patients undergoing surgery with general anesthesia. To our knowledge, there is no study examining TFPB in donor nephrectomy.

The investigators aimed to prospectively examine the effect of TFPB and RSB on opioid consumption in postoperative period on donors who will undergo laparoscopic nephrectomy in renal transplantation surgery.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Donor patients scheduled for elective nephrectomy in renal transplantation surgery
  • American Society of Anesthesiologists (ASA) I-II
  • Patients who are aged between 18-75
Exclusion Criteria
  • Skin infection at the block area
  • Coagulation disorder and using anticoagulant drugs
  • End-stage organ and system failure
  • Severe pulmonary and/or cardiovascular problems
  • Substance addiction or known psychiatric or mental problems
  • Chronic painkiller usage

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Transversalis Fascia Plane Block and Rectus Sheath Block GroupTransversalis fascia plane block and rectus sheath blockTransversalis Fascia Plane Block and Rectus Sheath Block will be administered to this group.
Transversalis Fascia Plane Block and Rectus Sheath Block GroupIntravenous fentanyl patient control deviceTransversalis Fascia Plane Block and Rectus Sheath Block will be administered to this group.
Control GroupIntravenous fentanyl patient control deviceNo regional anesthesia technique will be applied to the control group.
Primary Outcome Measures
NameTimeMethod
Total opioid consumption retrieved from patient recordsup to 24 hours

the amount of fentanyl required by the patient and given by the device will be recorded for the first 24 hours.

Secondary Outcome Measures
NameTimeMethod
Numeric Rating Scale (NRS)up to 24 hours

Pain of patients will be evaluated and recorded according to NRS. A NRS requires the patient to rate their pain on a defined scale between 0 and10 (0 is no pain and 10 is the worst pain)

Trial Locations

Locations (1)

Koç University Hospital

🇹🇷

Istanbul, Zeytinburnu, Turkey

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