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Nerve Block for Pain Relief After Robotic Kidney Cancer Surgery

Tests a nerve block for pain after robotic partial kidney removal in adults.

Plain-language title generated from the registry record
Registry title: QLESP Block for Pain Control in Robotic Partial Nephrectomy

Key facts

Where
Wuhan, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07704970, who can take part

Where in China

  • Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyWuhan, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Huazhong University of Science and Technology
Trial code
NCT07704970
Record updated
25 September 2026
Original description
The goal of this clinical trial is to learn if an ultrasound-guided nerve block called QLESP works to reduce pain and the need for strong pain medicines after robotic kidney surgery in adults. The main questions it aims to answer are:Read full original descriptionShow less

Ultrasound-Guided L2 Level QLESP Block for Postoperative Analgesia in Robot-Assisted Partial Nephrectomy: A Prospective Randomized Controlled Trial

The goal of this clinical trial is to learn if an ultrasound-guided nerve block called QLESP works to reduce pain and the need for strong pain medicines after robotic kidney surgery in adults. The main questions it aims to answer are:

1. Does QLESP reduce the total amount of opioid pain medicine participants need in the first 48 hours after surgery? 2. Does QLESP lower pain scores and improve recovery quality after surgery? Researchers will compare participants who receive QLESP block to participants who receive the same numbing medicine injected only at the surgical wound sites.

Participants will:

1. Be randomly assigned to receive either QLESP or local wound injection before surgery. 2. Have a patient-controlled pain pump for 48 hours after surgery. 3. Complete pain scores and recovery quality questionnaires at 2, 6, 12, 24, 48, and 72 hours after surgery. 4. Be followed until hospital discharge.

Inclusion: Aged 18 to 75 years; Scheduled for elective robot-assisted partial nephrectomy (RAPN); American Society of Anesthesiologists (ASA) physical status I to III; Body mass index (BMI) 18 to 35 kg/m²; Voluntarily signed informed consent form Able to understand pain scoring and use of patient-controlled analgesia (PCA).

Exclusion: Use of analgesic medications within the past 3 months; Infection at the intended puncture site; Coagulopathy or bleeding diathesis; Known allergy or contraindication to local anesthetics or opioids; Severe cardiac, hepatic, or renal dysfunction; Language, communication, or comprehension barriers; Peripheral neuropathy; Pregnancy or breastfeeding; Refusal to participate in the study.

ClinicalTrials.gov NCT07704970