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The analgesic effect of ultrasound-guided transversus abdominis plane block in partial or radical nephrectomy

The analgesic effect of ultrasound-guided transversus abdominis plane block in partial or radical nephrectomy: a prospective, randomized, blinded, placebo-controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013244
Enrollment
Unknown
Registered
2017-11-04
Start date
2018-01-01
Completion date
Unknown
Last updated
2017-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

kidney disease

Interventions

Intervention Group:transversus abdominis plane block with ropivacaine
Control Group:transversus abdominis plane block with normal saline

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged between 18 and 70 years who were scheduled to undergo elective laparoscopic /robot-assisted partial or radical nephrectomy; 2. Patients who assigned the informed consent document before surgery.;Inclusion criteria: 1. Patients aged between 18 and 70 years who were scheduled to undergo elective laparoscopic /robot-assisted partial or radical nephrectomy; 2. Patients who assigned the informed consent document before surgery.;Inclusion criteria: 1. Patients aged between 18 and 70 years who were scheduled to undergo elective laparoscopic /robot-assisted partial or radical nephrectomy; 2. Patients who assigned the informed consent document before surgery.;Inclusion criteria: 1. Patients aged between 18 and 70 years who were scheduled to undergo elective laparoscopic /robot-assisted partial or radical nephrectomy; 2. Patients who assigned the informed consent document before surgery.;Inclusion criteria: 1. Patients aged between 18 and 70 years who were scheduled to undergo elective laparoscopic /robot-assisted partial or radical nephrectomy; 2. Patients who assigned the informed consent document before surgery.

Exclusion criteria

Exclusion criteria: 1. Refuse to participate; 2. Chronic opium-addiction and take other kind of analgesic drugs beyond 3 months; 3. Unable to communicate due to severe dementia, language barrier or end-stage disease; 4. Allergic to local anesthetics; 5. Nerve block contraindication such as infection in the puncture site or severe coagulation dysfunction; 6. Any other conditions that are considered unsuitable for study participation.;Exclusion criteria: 1. Refuse to participate; 2. Chronic opium-addiction and take other kind of analgesic drugs beyond 3 months; 3. Unable to communicate due to severe dementia, language barrier or end-stage disease; 4. Allergic to local anesthetics; 5. Nerve block contraindication such as infection in the puncture site or severe coagulation dysfunction; 6. Any other conditions that are considered unsuitable for study participation.;Exclusion criteria: 1. Refuse to participate; 2. Chronic opium-addiction and take other kind of analgesic drugs beyond 3 months; 3. Unable to communicate due to severe dementia, language barrier or end-stage disease; 4. Allergic to local anesthetics; 5. Nerve block contraindication such as infection in the puncture site or severe coagulation dysfunction; 6. Any other conditions that are considered unsuitable for study participation.;Exclusion criteria: 1. Refuse to participate; 2. Chronic opium-addiction and take other kind of analgesic drugs beyond 3 months; 3. Unable to communicate due to severe dementia, language barrier or end-stage disease; 4. Allergic to local anesthetics; 5. Nerve block contraindication such as infection in the puncture site or severe coagulation dysfunction; 6. Any other conditions that are considered unsuitable for study participation.;Exclusion criteria: 1. Refuse to participate; 2. Chronic opium-addiction and take other kind of analgesic drugs beyond 3 months; 3. Unable to communicate due to severe dementia, language barrier or end-stage disease; 4. Allergic to local anesthetics; 5. Nerve block contraindication such as infection in the puncture site or severe coagulation dysfunction; 6. Any other conditions that are considered unsuitable for study participation.

Design outcomes

Primary

MeasureTime frame
the amount of opioid drugs used during the anesthesia period;the amount of opioid drugs used in the first 24 hours after surgery;

Secondary

MeasureTime frame
NRS pain score;the incidence of postoperative nausea and vomiting;the time interval for the first bolus opioid after surgery;the length of stay in hospital after surgery;

Countries

China

Contacts

Public ContactZengmao Lin;Zengmao Lin;Zengmao Lin;Zengmao Lin;Zengmao Lin ;;;;

Peking University First Hospital;Peking University First Hospital;Peking University First Hospital;Peking University First Hospital;Peking University First Hospital

13810098351@163.com;13810098351@163.com;13810098351@163.com;13810098351@163.com;13810098351@163.com+86 13810098351;+86 13810098351;+86 13810098351;+86 13810098351;+86 13810098351

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 1, 2026